MeCP2 Affects Skeletal Muscle Growth and Morphology through Non Cell-Autonomous Mechanisms.

Rett syndrome (RTT) is an autism spectrum disorder mainly caused by mutations in the X-linked MECP2 gene and affecting roughly 1 out of 10.000 born girls. Symptoms range in severity and include stereotypical movement, lack of spoken language, seizures, ataxia and severe intellectual disability. Nota...

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Bibliographic Details
Main Authors: Valentina Conti, Anna Gandaglia, Francesco Galli, Mario Tirone, Elisa Bellini, Lara Campana, Charlotte Kilstrup-Nielsen, Patrizia Rovere-Querini, Silvia Brunelli, Nicoletta Landsberger
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4476581?pdf=render