Simvastatin offers new prospects for the treatment of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is the most common and severe inherited neuromuscular disorder. DMD is caused by mutations in the gene encoding the dystrophin protein in muscle fibers. Dystrophin was originally proposed to be a structural protein that protected the sarcolemma from stresses produce...

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Detalles Bibliográficos
Autores principales: Whitehead, Nicholas P., Kim, Min Jeong, Bible, Kenneth L., Adams, Marvin E., Froehner, Stanley C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838314/
https://www.ncbi.nlm.nih.gov/pubmed/27141415
http://dx.doi.org/10.1080/21675511.2016.1156286

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838314/
https://www.ncbi.nlm.nih.gov/pubmed/27141415
http://dx.doi.org/10.1080/21675511.2016.1156286

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