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- W2044763721 abstract "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 apparently normal early infancy. In addition, MECP2 mutations and duplications are observed in a spectrum of neurodevelopmental disorders, including severe neonatal encephalopathy, X-linked mental retardation, and autism, implicating MeCP2 as an essential regulator of postnatal brain development. In this review, we compare the mutation types and inheritance patterns of the human disorders associated with MECP2. In addition, we summarize the current understanding of MeCP2 as a central epigenetic regulator of activity-dependent synaptic maturation. As MeCP2 occupies a central role in the pathogenesis of multiple neurodevelopmental disorders, continued investigation into MeCP2 function and regulatory pathways may show promise for developing broad-spectrum therapies." @default.
- W2044763721 created "2016-06-24" @default.
- W2044763721 creator A5010417321 @default.
- W2044763721 creator A5051358401 @default.
- W2044763721 date "2010-03-24" @default.
- W2044763721 modified "2023-09-30" @default.
- W2044763721 title "The Role of MeCP2 in Brain Development and Neurodevelopmental Disorders" @default.
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- W2044763721 doi "https://doi.org/10.1007/s11920-010-0097-7" @default.
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