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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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Conti, Valentina, Gandaglia, Anna, Galli, Francesco, Tirone, Mario, Bellini, Elisa, Campana, Lara, Kilstrup-Nielsen, Charlotte, Rovere-Querini, Patrizia, Brunelli, Silvia, Landsberger, Nicoletta
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4476581/
https://ncbi.nlm.nih.gov/pubmed/26098633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0130183
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