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Clinical aspects, molecular pathomechanisms and management of myotonic dystrophies
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal dominant progressive myopathy, myotonia and multiorgan involvement. To date two distinct forms caused by similar mutations have been identified. Myotonic dystrophy type 1 (DM1, Steinert's disease) wa...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Pacini Editore SpA
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006279/ https://www.ncbi.nlm.nih.gov/pubmed/24803843 |