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Antisense oligonucleotides for the treatment of cardiomyopathy in Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is an X-linked recessive fatal neuromuscular disorder characterized by progressive muscle degeneration which affects one in 3500-5000 males born worldwide. DMD is caused by loss-of-function mutations in the dystrophin (DMD) gene encoding for dystrophin, a cytoskelet...

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Bibliografski detalji
Izdano u:Am J Transl Res
Glavni autori: Nguyen, Quynh, Yokota, Toshifumi
Format: Artigo
Jezik:Inglês
Izdano: e-Century Publishing Corporation 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6456507/
https://ncbi.nlm.nih.gov/pubmed/30972156
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