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Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears
Facioscapulohumeral muscular dystrophy (FSHD) has been classified as an autosomal dominant myopathy, linked to rearrangements in an array of 3.3 kb tandemly repeated DNA elements (D4Z4) located at the 4q subtelomere (4q35). For the last 20 years, the diagnosis of FSHD has been confirmed in clinical...
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| 發表在: | Curr Mol Med |
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| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Bentham Science Publishers
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4264243/ https://ncbi.nlm.nih.gov/pubmed/25323867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1566524014666141010155054 |
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