Antisense oligonucleotides for the treatment of cardiomyopathy in Duchenne muscular dystrophy.

Duchenne muscular dystrophy antisense therapy cardiomyopathy drug delivery dystrophin morpholinos

Journal

American journal of translational research
ISSN: 1943-8141
Titre abrégé: Am J Transl Res
Pays: United States
ID NLM: 101493030

Informations de publication

Date de publication:
2019
Historique:
received: 19 09 2018
accepted: 02 01 2019
entrez: 12 4 2019
pubmed: 12 4 2019
medline: 12 4 2019
Statut: epublish

Résumé

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

Identifiants

pubmed: 30972156
pmc: PMC6456507

Types de publication

Journal Article Review

Langues

eng

Pagination

1202-1218

Déclaration de conflit d'intérêts

None.

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Auteurs

Quynh Nguyen (Q)

Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta 8812-112 St., Edmonton, AB T6G 2H7, Canada.

Toshifumi Yokota (T)

Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta 8812-112 St., Edmonton, AB T6G 2H7, Canada.
The Friends of Garret Cumming Research and Muscular Dystrophy Canada HM Toupin Neurological Science Research Chair 8812-112 St., Edmonton, AB T6G 2H7, Canada.

Classifications MeSH