From diagnosis to therapy in Duchenne muscular dystrophy

Genetic approaches for the diagnosis and treatment of inherited muscle diseases have advanced rapidly in recent years. Many of the advances have occurred in the treatment of Duchenne muscular dystrophy (DMD), a muscle wasting disease where affected boys are typically wheelchair bound by age 12 years...

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Detalles Bibliográficos
Autores principales: Babbs, Arran, Chatzopoulou, Maria, Edwards, Ben, Squire, Sarah E., Wilkinson, Isabel V.L., Wynne, Graham M., Russell, Angela J., Davies, Kay E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329342/
https://www.ncbi.nlm.nih.gov/pubmed/32597486
http://dx.doi.org/10.1042/BST20190282

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329342/
https://www.ncbi.nlm.nih.gov/pubmed/32597486
http://dx.doi.org/10.1042/BST20190282

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