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<title>Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Māori Population - GeneReviews® - NCBI Bookshelf</title>
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<meta name="robots" content="INDEX,FOLLOW,NOARCHIVE" /><meta name="citation_inbook_title" content="GeneReviews® [Internet]" /><meta name="citation_title" content="Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Māori Population" /><meta name="citation_publisher" content="University of Washington, Seattle" /><meta name="citation_date" content="2023/01/12" /><meta name="citation_author" content="Stephanie E Wallace" /><meta name="citation_fulltext_html_url" content="https://www.ncbi.nlm.nih.gov/books/NBK588573/" /><link rel="schema.DC" href="http://purl.org/DC/elements/1.0/" /><meta name="DC.Title" content="Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Māori Population" /><meta name="DC.Type" content="Text" /><meta name="DC.Publisher" content="University of Washington, Seattle" /><meta name="DC.Contributor" content="Stephanie E Wallace" /><meta name="DC.Date" content="2023/01/12" /><meta name="DC.Identifier" content="https://www.ncbi.nlm.nih.gov/books/NBK588573/" /><meta name="description" content="A founder variant is a pathogenic variant observed at high frequency in a specific population due to the presence of the variant in a single ancestor or small number of ancestors. The presence of a founder variant can affect the approach to molecular genetic testing. When one or more founder variants account for a large percentage of all pathogenic variants found in a population, testing for the founder variant(s) may be performed first." /><meta name="og:title" content="Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Māori Population" /><meta name="og:type" content="book" /><meta name="og:description" content="A founder variant is a pathogenic variant observed at high frequency in a specific population due to the presence of the variant in a single ancestor or small number of ancestors. The presence of a founder variant can affect the approach to molecular genetic testing. When one or more founder variants account for a large percentage of all pathogenic variants found in a population, testing for the founder variant(s) may be performed first." /><meta name="og:url" content="https://www.ncbi.nlm.nih.gov/books/NBK588573/" /><meta name="og:site_name" content="NCBI Bookshelf" /><meta name="og:image" content="https://www.ncbi.nlm.nih.gov/corehtml/pmc/pmcgifs/bookshelf/thumbs/th-gene-lrg.png" /><meta name="twitter:card" content="summary" /><meta name="twitter:site" content="@ncbibooks" /><meta name="bk-non-canon-loc" content="/books/n/gene/founder_maori/" /><link rel="canonical" href="https://www.ncbi.nlm.nih.gov/books/NBK588573/" /><link rel="stylesheet" href="/corehtml/pmc/css/figpopup.css" type="text/css" media="screen" /><link rel="stylesheet" href="/corehtml/pmc/css/bookshelf/2.26/css/books.min.css" type="text/css" /><link rel="stylesheet" href="/corehtml/pmc/css/bookshelf/2.26/css/books_print.min.css" type="text/css" /><style type="text/css">p a.figpopup{display:inline !important} .bk_tt {font-family: monospace} .first-line-outdent .bk_ref {display: inline} </style><script type="text/javascript" src="/corehtml/pmc/js/jquery.hoverIntent.min.js"> </script><script type="text/javascript" src="/corehtml/pmc/js/common.min.js?_=3.18"> </script><script type="text/javascript">window.name="mainwindow";</script><script type="text/javascript" src="/corehtml/pmc/js/bookshelf/2.26/book-toc.min.js"> </script><script type="text/javascript" src="/corehtml/pmc/js/bookshelf/2.26/books.min.js"> </script><script type="text/javascript">if (typeof (jQuery) != 'undefined') { (function ($) { $(function () { var min = Math.ceil(1); var max = Math.floor(100000); var randomNum = Math.floor(Math.random() * (max - min)) + min; var surveyUrl = "/projects/Gene/portal/surveys/seqdbui-survey.js?rando=" + randomNum.toString(); $.getScript(surveyUrl, function () { try { ncbi.seqDbUISurvey.init(); } catch (err) { console.info(err); } }).fail(function (jqxhr, settings, exception) { console.info('Cannot load survey script', jqxhr); });; }); })(jQuery); };</script>
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<div class="pre-content"><div><div class="bk_prnt"><p class="small">NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.</p><p>Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2025. </p></div></div></div>
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<div class="main-content lit-style" itemscope="itemscope" itemtype="http://schema.org/CreativeWork"><div class="meta-content fm-sec"><h1 id="_NBK588573_"><span class="title" itemprop="name">Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Māori Population</span></h1><div class="contrib half_rhythm"><span itemprop="author">Stephanie E Wallace</span>, MD<div class="affiliation small">Senior Editor, <i>GeneReviews</i></div><div class="affiliation small">Clinical Professor, Department of Pediatrics<br />University of Washington<br />Seattle, Washington<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="ude.wu@2rotide" class="oemail">ude.wu@2rotide</a></div></div></div><p class="small">Initial Posting: <span itemprop="datePublished">January 12, 2023</span>.</p><p><em>Estimated reading time: 1 minute</em></p></div><div class="body-content whole_rhythm" itemprop="text"><p>A founder variant is a pathogenic variant observed at high frequency in a specific population due to the presence of the variant in a single ancestor or small number of ancestors. The presence of a founder variant can affect the approach to molecular genetic testing. When one or more founder variants account for a large percentage of all pathogenic variants found in a population, testing for the founder variant(s) may be performed first.</p><p>The table below includes common founder variants – here defined as <b>three or fewer variants that account for >50% of the pathogenic variants identified in a single gene in individuals of a specific ancestry</b> – in individuals of Māori ancestry. Note: Pathogenic variants that are common worldwide due to a DNA sequence hot spot are not considered founder variants and thus are not included.</p><div id="founder_maori.T.genetic_disorders_associ" class="table"><h3><span class="label">Table. </span></h3><div class="caption"><p>Genetic Disorders Associated with Founder Variants Common in the Māori Population</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK588573/table/founder_maori.T.genetic_disorders_associ/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__founder_maori.T.genetic_disorders_associ_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Disorder</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">MOI</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">DNA Nucleotide Change</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Predicted Protein Change</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">% of Pathogenic Variants in Gene <sup>1</sup></th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_7" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Carrier Frequency</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_8" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Ethnicity</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_9" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Reference Sequences</th><th id="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_10" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">References</th></tr></thead><tbody><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>ADAMTSL4</i>
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</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Ectopia lentis (See <a href="/books/n/gene/adamtsl4-eyes/"><i>ADAMTSL4</i>-Related Eye Disorders</a>.)</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.2237G>A</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Arg746His</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">~100% <sup>2</sup></td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_7" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">1/132</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_8" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Māori</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_9" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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||
<a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_019032.6" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_019032<wbr style="display:inline-block"></wbr>.6</a>
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<br />
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<a href="https://www.ncbi.nlm.nih.gov/protein/NP_061905.2" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_061905<wbr style="display:inline-block"></wbr>.2</a>
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||
</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_10" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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||
<a class="bk_pop" href="#founder_maori.REF.van_bysterveldt.2017.537">van Bysterveldt et al [2017]</a>
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||
</td></tr><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_1" rowspan="4" scope="row" colspan="1" style="text-align:left;vertical-align:middle;">
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||
<i>CDH1</i>
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</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_2" rowspan="4" colspan="1" style="text-align:left;vertical-align:middle;">
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||
<a href="/books/n/gene/hgc/">Hereditary diffuse gastric cancer</a>
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||
</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_3" rowspan="4" colspan="1" style="text-align:left;vertical-align:middle;">AD</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.190C>T</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Gln64Ter</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">24%</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_7" rowspan="4" colspan="1" style="text-align:left;vertical-align:middle;">NA</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_8" rowspan="4" colspan="1" style="text-align:left;vertical-align:middle;">Māori</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_9" rowspan="4" colspan="1" style="text-align:left;vertical-align:middle;">
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||
<a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_004360.5" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_004360<wbr style="display:inline-block"></wbr>.5</a>
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<br />
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||
<a href="https://www.ncbi.nlm.nih.gov/protein/NP_004351.1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_004351<wbr style="display:inline-block"></wbr>.1</a>
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||
</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_10" rowspan="4" colspan="1" style="text-align:left;vertical-align:middle;">
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||
<a class="bk_pop" href="#founder_maori.REF.hakkaart.2019.83">Hakkaart et al [2019]</a>
|
||
</td></tr><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">c.1792C>T</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Arg598Ter</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">24%</td></tr><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">c.2287G>T</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Glu763Ter</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">24%</td></tr><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">c.2386dupC</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Arg796ProfsTer11</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">24%</td></tr><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
||
<i>NPHS1</i>
|
||
</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Congenital nephrotic syndrome (OMIM <a href="https://omim.org/entry/256300" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">256300</a>)</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.2131C>A</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Arg711Ser</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">82%</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_7" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Unknown</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_8" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Māori</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_9" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
||
<a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_004646.4" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_004646<wbr style="display:inline-block"></wbr>.4</a>
|
||
<br />
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||
<a href="https://www.ncbi.nlm.nih.gov/protein/NP_004637.1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_004637<wbr style="display:inline-block"></wbr>.1</a>
|
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</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_10" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
||
<a class="bk_pop" href="#founder_maori.REF.wong.2013.2313">Wong et al [2013]</a>
|
||
</td></tr><tr><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
||
<i>PDE6B</i>
|
||
</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Retinitis pigmentosa 40 (OMIM <a href="https://omim.org/entry/613801" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">613801</a>)</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.2197G>C</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Ala733Pro</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_6" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">~100% <sup>2</sup></td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_7" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">1/124</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_8" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Māori</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_9" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
||
<a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_000283.4" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_000283<wbr style="display:inline-block"></wbr>.4</a>
|
||
<br />
|
||
<a href="https://www.ncbi.nlm.nih.gov/protein/NP_000274.3" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_000274<wbr style="display:inline-block"></wbr>.3</a>
|
||
</td><td headers="hd_h_founder_maori.T.genetic_disorders_associ_1_1_1_10" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
||
<a class="bk_pop" href="#founder_maori.REF.vincent.2017.901">Vincent et al [2017]</a>
|
||
</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">Included if ≤3 pathogenic variants account for ≥50% of variants identified in a specific ethnic group</p></div></dd><dt></dt><dd><div><p class="no_margin">AD = autosomal dominant; AR = autosomal recessive; MOI = mode of inheritance; NA = not applicable</p></div></dd><dt>1. </dt><dd><div id="founder_maori.TF.e.1"><p class="no_margin">This percentage does not account for the possibility of rare <i>de novo</i> pathogenic variants occurring in this population.</p></div></dd><dt>2. </dt><dd><div id="founder_maori.TF.e.2"><p class="no_margin">To date, additional pathogenic variants in this gene have not been reported in individuals of Māori descent.</p></div></dd></dl></div></div></div><div id="founder_maori.References"><h2 id="_founder_maori_References_">References</h2><ul class="simple-list"><li class="half_rhythm"><div class="bk_ref" id="founder_maori.REF.hakkaart.2019.83">Hakkaart C, Ellison-Loschmann L, Day R, Sporle A, Koea J, Harawira P, Cheng S, Gray M, Whaanga T, Pearce N, Guilford P. Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori. <span><span class="ref-journal">Fam Cancer. </span>2019;<span class="ref-vol">18</span>:83–90.</span> [<a href="/pmc/articles/PMC6323075/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC6323075</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/29589180" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 29589180</span></a>]</div></li><li class="half_rhythm"><div class="bk_ref" id="founder_maori.REF.van_bysterveldt.2017.537">van Bysterveldt KA, Al Taie R, Ikink W, Oliver VF, Vincent AL. ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians. <span><span class="ref-journal">Ophthalmic Genet. </span>2017;<span class="ref-vol">38</span>:537–43.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/28394649" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28394649</span></a>]</div></li><li class="half_rhythm"><div class="bk_ref" id="founder_maori.REF.vincent.2017.901">Vincent AL, Abeysekera N, van Bysterveldt KA, Oliver VF, Ellingford JM, Barton S, Black GC. Next-generation sequencing targeted disease panel in rod-cone retinal dystrophies in Māori and Polynesian reveals novel changes and a common founder mutation. <span><span class="ref-journal">Clin Exp Ophthalmol. </span>2017;<span class="ref-vol">45</span>:901–10.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/28488341" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28488341</span></a>]</div></li><li class="half_rhythm"><div class="bk_ref" id="founder_maori.REF.wong.2013.2313">Wong W, Morris MC, Kara T. Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy. <span><span class="ref-journal">Pediatr Nephrol. </span>2013;<span class="ref-vol">28</span>:2313–21.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/23949594" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23949594</span></a>]</div></li></ul></div><div id="founder_maori.Revision_History"><h2 id="_founder_maori_Revision_History_">Revision History</h2><ul><li class="half_rhythm"><div>12 January 2023 (sw) Initial posting</div></li></ul></div><div id="bk_toc_contnr"></div></div></div>
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