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Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
In facioscapulohumeral muscular dystrophy (FSHD) the majority of patients carry a D4Z4 macrosatellite repeat contraction in the subtelomere of chromosome 4q. Several disease mechanisms have been proposed to explain how repeat contraction causes muscular dystrophy. All proposed mechanisms foresee a c...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2987013/ https://ncbi.nlm.nih.gov/pubmed/19809486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.62 |
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