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MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome (RTT), a rare neurodevelopmental disorder with a notable period of developmental regression following apparently normal initial development. Such MeCP2 alterations often result in changes to DNA binding and chroma...

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Detalles Bibliográficos
Autores principales:	Good, Katrina V., Vincent, John B., Ausió, Juan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859524/ https://www.ncbi.nlm.nih.gov/pubmed/33552148 http://dx.doi.org/10.3389/fgene.2021.620859

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