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Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism

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) is caus...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Neuromuscul Dis
Prif Awduron: Meola, Giovanni, Cardani, Rosanna
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: IOS Press 2015
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5240594/
https://ncbi.nlm.nih.gov/pubmed/27858759
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JND-150088
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