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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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Dades bibliogràfiques
Publicat a:Dis Model Mech
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: The Company of Biologists Ltd 2021
Matèries:
Accés en línia: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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