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...

Descripción completa

Detalles Bibliográficos
Autores principales: Conti, Valentina, Gandaglia, Anna, Galli, Francesco, Tirone, Mario, Bellini, Elisa, Campana, Lara, Kilstrup-Nielsen, Charlotte, Rovere-Querini, Patrizia, Brunelli, Silvia, Landsberger, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476581/
https://www.ncbi.nlm.nih.gov/pubmed/26098633
http://dx.doi.org/10.1371/journal.pone.0130183

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476581/
https://www.ncbi.nlm.nih.gov/pubmed/26098633
http://dx.doi.org/10.1371/journal.pone.0130183

Ejemplares similares