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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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Bibliografische gegevens
Gepubliceerd in:Oxid Med Cell Longev
Hoofdauteurs: Kuno, Atsushi, Horio, Yoshiyuki
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi Publishing Corporation 2016
Onderwerpen:
Online toegang: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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