Muscle wasting in myotonic dystrophies: a model of premature aging

Myotonic dystrophy type 1 (DM1 or Steinert’s disease) and type 2 (DM2) are multisystem disorders of genetic origin. Progressive muscular weakness, atrophy and myotonia are the most prominent neuromuscular features of these diseases, while other clinical manifestations such as cardiomyopathy, insulin...

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Detalles Bibliográficos
Autores principales: Mateos-Aierdi, Alba Judith, Goicoechea, Maria, Aiastui, Ana, Fernández-Torrón, Roberto, Garcia-Puga, Mikel, Matheu, Ander, López de Munain, Adolfo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496580/
https://www.ncbi.nlm.nih.gov/pubmed/26217220
http://dx.doi.org/10.3389/fnagi.2015.00125

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496580/
https://www.ncbi.nlm.nih.gov/pubmed/26217220
http://dx.doi.org/10.3389/fnagi.2015.00125

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