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Pathogenic mechanisms of myotonic dystrophy
DM (myotonic dystrophy) is a dominantly inherited genetic disorder that is the most common cause of muscular dystrophy in adults affecting 1 in 8500 individuals worldwide. Different microsatellite expansions in two loci cause different forms of the disease that share similar features: DM1 (DM type 1...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3873089/ https://ncbi.nlm.nih.gov/pubmed/19909263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST0371281 |
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