Cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD). Better understanding of molecular pathways leading to DMD fibrosis may provide novel targets for drug therapy. Matrix metalloproteinases… Click to show full abstract
Cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD). Better understanding of molecular pathways leading to DMD fibrosis may provide novel targets for drug therapy. Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) regulate collagen
               
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