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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zimmermann, Christoph A., Hoffmann, Anke, Raabe, Florian, Spengler, Dietmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377834/
https://www.ncbi.nlm.nih.gov/pubmed/25756305
http://dx.doi.org/10.3390/genes6010060

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377834/
https://www.ncbi.nlm.nih.gov/pubmed/25756305
http://dx.doi.org/10.3390/genes6010060

Ejemplares similares