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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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Detalles Bibliográficos
Publicado en:Dis Model Mech
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado: The Company of Biologists Ltd 2021
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Acceso en liña: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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