Dystromirs as Serum Biomarkers for Monitoring the Disease Severity in Duchenne Muscular Dystrophy

Duchenne muscular Dystrophy (DMD) is an inherited disease caused by mutations in the dystrophin gene that disrupt the open reading frame, while in frame mutations result in Becker muscular dystrophy (BMD). Ullrich congenital muscular dystrophy (UCMD) is due to mutations affecting collagen VI genes....

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Detalles Bibliográficos
Autores principales: Zaharieva, Irina T., Calissano, Mattia, Scoto, Mariacristina, Preston, Mark, Cirak, Sebahattin, Feng, Lucy, Collins, James, Kole, Ryszard, Guglieri, Michela, Straub, Volker, Bushby, Kate, Ferlini, Alessandra, Morgan, Jennifer E., Muntoni, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840009/
https://www.ncbi.nlm.nih.gov/pubmed/24282529
http://dx.doi.org/10.1371/journal.pone.0080263

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840009/
https://www.ncbi.nlm.nih.gov/pubmed/24282529
http://dx.doi.org/10.1371/journal.pone.0080263

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