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Skeletal Muscle Fibrosis in the mdx/utrn+/- Mouse Validates Its Suitability as a Murine Model of Duchenne Muscular Dystrophy

Various therapeutic approaches have been studied for the treatment of Duchenne muscular dystrophy (DMD), but none of these approaches have led to significant long-term effects in patients. One reason for this observed inefficacy may be the use of inappropriate animal models for the testing of therap...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Gutpell, Kelly M., Hrinivich, William T., Hoffman, Lisa M.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4301874/
https://ncbi.nlm.nih.gov/pubmed/25607927
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0117306
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