Cardiovascular phenotype of the Dmd(mdx) rat – a suitable animal model for Duchenne muscular dystrophy

Besides skeletal muscle abnormalities, Duchenne muscular dystrophy (DMD) patients present with dilated cardiomyopathy development, which considerably contributes to morbidity and mortality. Because the mechanisms responsible for the cardiac complications in the context of DMD are largely unknown, ev...

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Bibliografische gegevens
Gepubliceerd in:Dis Model Mech
Hoofdauteurs: Szabó, Petra Lujza, Ebner, Janine, Koenig, Xaver, Hamza, Ouafa, Watzinger, Simon, Trojanek, Sandra, Abraham, Dietmar, Todt, Hannes, Kubista, Helmut, Schicker, Klaus, Remy, Séverine, Anegon, Ignacio, Kiss, Attila, Podesser, Bruno K., Hilber, Karlheinz
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The Company of Biologists Ltd 2021
Onderwerpen:
Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7927653/
https://ncbi.nlm.nih.gov/pubmed/33619211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.047704
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