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Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome–like phenotypes
Mutations in the X-linked gene encoding methyl-CpG–binding protein 2 (MeCP2) cause Rett syndrome (RTT), a neurological disorder affecting cognitive development, respiration, and motor function. Genetic restoration of MeCP2 expression reverses RTT-like phenotypes in mice, highlighting the need to sea...
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| 出版年: | J Clin Invest |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5409785/ https://ncbi.nlm.nih.gov/pubmed/28394263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI90967 |
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