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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Detalles Bibliográficos
Autores principales: Meola, Giovanni, Cardani, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2015
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240594/
https://www.ncbi.nlm.nih.gov/pubmed/27858759
http://dx.doi.org/10.3233/JND-150088

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240594/
https://www.ncbi.nlm.nih.gov/pubmed/27858759
http://dx.doi.org/10.3233/JND-150088

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