Dystrophin is required for the normal function of the cardio-protective K(ATP) channel in cardiomyocytes.
Duchenne and Becker muscular dystrophy patients often develop a cardiomyopathy for which the pathogenesis is still unknown. We have employed the murine animal model of Duchenne muscular dystrophy (mdx), which develops a cardiomyopathy that includes some characteristics of the human disease, to study...
Main Authors: | Laura Graciotti, Jodi Becker, Anna Luisa Granata, Antonio Domenico Procopio, Lino Tessarollo, Gianluca Fulgenzi |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-01-01
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Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3205025?pdf=render |
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