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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Detalles Bibliográficos
Autores principales: Denny, Adam Philip, Heather, Alison Kay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485364/
https://www.ncbi.nlm.nih.gov/pubmed/28690764
http://dx.doi.org/10.1155/2017/7020295

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485364/
https://www.ncbi.nlm.nih.gov/pubmed/28690764
http://dx.doi.org/10.1155/2017/7020295

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