Duchenne Muscular Dystrophy: From Diagnosis to Therapy

Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder due to mutations in the dystrophin gene. It is characterized by progressive muscle weakness and wasting due to the absence of dystrophin protein that causes degeneration of skeletal and cardiac muscle. The molecular di...

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Detalles Bibliográficos
Autores principales: Falzarano, Maria Sofia, Scotton, Chiara, Passarelli, Chiara, Ferlini, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332113/
https://www.ncbi.nlm.nih.gov/pubmed/26457695
http://dx.doi.org/10.3390/molecules201018168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332113/
https://www.ncbi.nlm.nih.gov/pubmed/26457695
http://dx.doi.org/10.3390/molecules201018168

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