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Cellular and molecular mechanisms underlying muscular dystrophy

The muscular dystrophies are a group of heterogeneous genetic diseases characterized by progressive degeneration and weakness of skeletal muscle. Since the discovery of the first muscular dystrophy gene encoding dystrophin, a large number of genes have been identified that are involved in various mu...

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Detalles Bibliográficos
Autores principales: Rahimov, Fedik, Kunkel, Louis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653356/
https://www.ncbi.nlm.nih.gov/pubmed/23671309
http://dx.doi.org/10.1083/jcb.201212142