SIRT1: A Novel Target for the Treatment of Muscular Dystrophies

Muscular dystrophies are inherited myogenic disorders accompanied by progressive skeletal muscle weakness and degeneration. Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular dystrophy and is caused by mutations in the gene that encodes the cytoskeletal protein dystroph...

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Detalles Bibliográficos
Autores principales: Kuno, Atsushi, Horio, Yoshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814699/
https://www.ncbi.nlm.nih.gov/pubmed/27073590
http://dx.doi.org/10.1155/2016/6714686

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814699/
https://www.ncbi.nlm.nih.gov/pubmed/27073590
http://dx.doi.org/10.1155/2016/6714686

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