Mutations in the human TWIST gene
- PMID: 10790211
- DOI: 10.1002/(SICI)1098-1004(200005)15:5<479::AID-HUMU10>3.0.CO;2-#
Mutations in the human TWIST gene
Abstract
The authors wish to correct a mistake in the amino acid change stemming from a 490C>T nucleotide change. In this article, the nucleotide change is stated to lead to a Q165X amino acid change. The 490C>T nucleotide change should actually cause a Q164X amino acid change.
Similar articles
-
Identification of P gene mutations in individuals with oculocutaneous albinism in sub-saharan africa; robyn kerr, gwynneth stevens, prashiela manga, sarah salm, premila john, tabitha haw, and michele ramsay; (Article was originally published in human mutation 15:166-172, 2000).Hum Mutat. 2000;16(1):87. doi: 10.1002/1098-1004(200007)16:1<87::AID-HUMU14>3.0.CO;2-P. Hum Mutat. 2000. PMID: 10874310
-
Four single-nucleotide polymorphisms in the human BUB1 gene.J Hum Genet. 2001;46(3):150-1. doi: 10.1007/PL00010920. J Hum Genet. 2001. PMID: 11310583
-
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.Mol Vis. 2006 Dec 1;12:1448-60. Mol Vis. 2006. PMID: 17167399
-
Gene conversion-like missense mutations in the human cationic trypsinogen gene and insights into the molecular evolution of the human trypsinogen family.Mol Genet Metab. 2000 Nov;71(3):463-9. doi: 10.1006/mgme.2000.3086. Mol Genet Metab. 2000. PMID: 11073713 Review.
-
Molecular advances in thyroglobulin disorders.Clin Chim Acta. 2006 Dec;374(1-2):8-24. doi: 10.1016/j.cca.2006.05.043. Epub 2006 Jun 7. Clin Chim Acta. 2006. PMID: 16870170 Review.
Cited by
-
Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening.Hum Genet. 2003 Dec;114(1):68-76. doi: 10.1007/s00439-003-1012-7. Epub 2003 Sep 25. Hum Genet. 2003. PMID: 14513358
-
Craniosynostosis: molecular pathways and future pharmacologic therapy.Organogenesis. 2012 Oct-Dec;8(4):103-13. doi: 10.4161/org.23307. Epub 2012 Oct 1. Organogenesis. 2012. PMID: 23249483 Free PMC article. Review.
-
Cell Mechanics of Craniosynostosis.ACS Biomater Sci Eng. 2017 Nov 13;3(11):2733-2743. doi: 10.1021/acsbiomaterials.6b00557. Epub 2016 Dec 14. ACS Biomater Sci Eng. 2017. PMID: 31106260 Free PMC article.
-
Genetic Causes of Craniosynostosis: An Update.Mol Syndromol. 2019 Feb;10(1-2):6-23. doi: 10.1159/000492266. Epub 2018 Aug 15. Mol Syndromol. 2019. PMID: 30976276 Free PMC article. Review.
-
Cranial Suture Regeneration Mitigates Skull and Neurocognitive Defects in Craniosynostosis.Cell. 2021 Jan 7;184(1):243-256.e18. doi: 10.1016/j.cell.2020.11.037. Cell. 2021. PMID: 33417861 Free PMC article.
LinkOut - more resources
Full Text Sources
Other Literature Sources