A review of Genetic Etiology and Emerging Molecular Therapies for FSHD in Preclinical Studies
Facioscapulohumeral muscular dystrophy is one of the most common musculoskeletal diseases with a considerable burden. Most of the affected individuals experience muscle weakness as the common muscular symptom. Despite the underlying genetic mechanism which is extensively studied, curative treatment...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Mashhad University of Medical Sciences
2021-03-01
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| Edice: | Reviews in Clinical Medicine |
| Témata: | |
| On-line přístup: | https://rcm.mums.ac.ir/article_18105_bb5add0c44a8170bb0fe6e734c973830.pdf |
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