Review
doi: 10.1086/345360.
Epub 2002 Nov 19.
Rett syndrome and MeCP2: linking epigenetics and neuronal function
Affiliations
- PMID: 12442230
- PMCID: PMC378559
- DOI: 10.1086/345360
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Review
Rett syndrome and MeCP2: linking epigenetics and neuronal function
Am J Hum Genet.
2002 Dec.
No abstract available
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References
Electronic-Database Information
-
- Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/ (for RTT [MIM 312750] and MeCP2 [MIM 300005])
References
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- Adler DA, Quaderi NA, Brown SD, Chapman VM, Moore J, Tate P, Disteche CM (1995) The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse. Mamm Genome 6:491–492 - PubMed
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- Akbarian S, Chen RZ, Gribnau J, Rasmussen TP, Fong H, Jaenisch R, Jones EG (2001) Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex. Neurobiol Dis 8:784–791 - PubMed
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- Amir R, Dahle EJ, Toriolo D, Zoghbi HY (2000a) Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in Xq. Am J Med Genet 90:69–71 - PubMed
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- Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ, Philippi A, Timar L, Percy AK, Motil KJ, Lichtarge O, Smith EO, Glaze DG, Zoghbi HY (2000b) Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann Neurol 47:670–679 - PubMed
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- Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23:185–188 - PubMed
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