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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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Detaylı Bibliyografya
Yayımlandı:Biochem Soc Trans
Asıl Yazarlar: Babbs, Arran, Chatzopoulou, Maria, Edwards, Ben, Squire, Sarah E., Wilkinson, Isabel V.L., Wynne, Graham M., Russell, Angela J., Davies, Kay E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Portland Press Ltd. 2020
Konular:
Online Erişim: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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