Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference30 articles.
1. Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?
2. DNA methylation and Rett syndrome
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
4. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
5. Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
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