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Role of Mecp2 in Experience-Dependent Epigenetic Programming

Mutations in the X-linked gene MECP2, the founding member of a family of proteins recognizing and binding to methylated DNA, are the genetic cause of a devastating neurodevelopmental disorder in humans, called Rett syndrome. Available evidence suggests that MECP2 protein has a critical role in activ...

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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Zimmermann, Christoph A., Hoffmann, Anke, Raabe, Florian, Spengler, Dietmar
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4377834/
https://ncbi.nlm.nih.gov/pubmed/25756305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes6010060
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