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• W3100696869 abstract "Duchenne muscular dystrophy (DMD) is X-linked recessive myopathy caused by mutations in the dystrophin gene. Although conventional treatments have improved their prognosis, inevitable progressive cardiomyopathy is still the leading cause of death in patients with DMD. To explore novel therapeutic options, a suitable animal model with heart involvement has been warranted." @default.
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• W3100696869 date "2020-11-28" @default.
• W3100696869 modified "2023-10-02" @default.
• W3100696869 title "Age-Dependent Echocardiographic and Pathologic Findings in a Rat Model with Duchenne Muscular Dystrophy Generated by CRISPR/Cas9 Genome Editing" @default.
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• W3100696869 doi "https://doi.org/10.1536/ihj.20-372" @default.
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