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Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene
Rett syndrome (RTT) is a severe neurodevelopmental disorder that is usually caused by mutations in Methyl-CpG-binding Protein 2 (MECP2). Four of the eight common disease causing mutations in MECP2 are nonsense mutations and are responsible for over 35% of all cases of RTT. A strategy to overcome dis...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4383870/ https://ncbi.nlm.nih.gov/pubmed/25634563 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv030 |
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