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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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| Gepubliceerd in: | Oxid Med Cell Longev |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Hindawi Publishing Corporation
2016
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| 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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