Cargando...
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...
Gardado en:
| Publicado en: | Curr Mol Med |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Bentham Science Publishers
2014
|
| Assuntos: | |
| Acceso en liña: | 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 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|