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Are Antioxidants a Potential Therapy for FSHD? A Review of the Literature

Facioscapulohumeral muscular dystrophy (FSHD) is an inherited myopathy affecting approximately 1 in 7500 individuals worldwide. It is a progressive disease characterised by skeletal muscle weakness and wasting. A genetic mutation on the 4q35 chromosome results in the expression of the double homeobo...

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Detalhes bibliográficos
Publicado no:Oxid Med Cell Longev
Main Authors: Denny, Adam Philip, Heather, Alison Kay
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5485364/
https://ncbi.nlm.nih.gov/pubmed/28690764
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/7020295
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