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The role of MeCP2 in CNS development and function
Rett syndrome is a neurodevelopmental disorder that is a direct consequence of functional mutations in the methyl-CpG-binding protein-2 (MeCP2) gene, which has focused attention on epigenetic mechanisms in neurons. MeCP2 is widely believed to be a transcriptional repressor although it may have addit...
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| Auteurs principaux: | , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2010
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3077534/ https://ncbi.nlm.nih.gov/pubmed/20515694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yhbeh.2010.05.014 |
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