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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...
Gorde:
| Argitaratua izan da: | Oxid Med Cell Longev |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Hindawi
2017
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| Gaiak: | |
| Sarrera elektronikoa: | 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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