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Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy

Myotonic dystrophy type 1 (DM1) and 2 (DM2) are autosomal dominant degenerative neuromuscular disorders characterized by progressive skeletal muscle weakness, atrophy, and myotonia with progeroid features. Although both DM1 and DM2 are characterized by skeletal muscle dysfunction and also share othe...

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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: André, Laurène M., Ausems, C. Rosanne M., Wansink, Derick G., Wieringa, Bé
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5985300/
https://ncbi.nlm.nih.gov/pubmed/29892259
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2018.00368
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