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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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Bibliografski detalji
Izdano u:Oxid Med Cell Longev
Glavni autori: Kuno, Atsushi, Horio, Yoshiyuki
Format: Artigo
Jezik:Inglês
Izdano: Hindawi Publishing Corporation 2016
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4814699/
https://ncbi.nlm.nih.gov/pubmed/27073590
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/6714686
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