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The Role of MeCP2 in Brain Development and Neurodevelopmental Disorders
Methyl CpG binding protein-2 (MeCP2) is an essential epigenetic regulator in human brain development. Rett syndrome, the primary disorder caused by mutations in the X-linked MECP2 gene, is characterized by a period of cognitive decline and development of hand stereotypies and seizures following an a...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Current Science Inc.
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847695/ https://www.ncbi.nlm.nih.gov/pubmed/20425298 http://dx.doi.org/10.1007/s11920-010-0097-7 |