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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Bibliographic Details
Published in:Biochem Soc Trans
Main Authors: Babbs, Arran, Chatzopoulou, Maria, Edwards, Ben, Squire, Sarah E., Wilkinson, Isabel V.L., Wynne, Graham M., Russell, Angela J., Davies, Kay E.
Format: Artigo
Language:Inglês
Published: Portland Press Ltd. 2020
Subjects:
Review Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7329342/
https://ncbi.nlm.nih.gov/pubmed/32597486
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20190282
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