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Evolving role of MeCP2 in Rett syndrome and autism
Rett syndrome is an X-linked autism-spectrum disorder caused by mutations in MECP2, encoding methyl CpG-binding protein 2. Since the discovery of MECP2 mutations as the genetic cause of Rett syndrome, the understanding of MeCP2 function has evolved. Although MeCP2 was predicted to be a global transc...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2867478/ https://ncbi.nlm.nih.gov/pubmed/20473347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2217/epi.09.13 |
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