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CRISPR-Cas9 generated Pompe knock-in murine model exhibits early-onset hypertrophic cardiomyopathy and skeletal muscle weakness

2019-09-24

Abstract excerpt

Infantile-onset Pompe Disease (IOPD), caused by mutations in lysosomal acid alpha-glucosidase ( Gaa ), manifests rapidly progressive fatal cardiac and skeletal myopathy incompletely attenuated by synthetic GAA intravenous infusions. The currently available murine model does not fully simulate human IOPD, displaying skeletal myopathy with late-onset hypertrophic cardiomyopathy. Bearing a Cre- LoxP induced exonic...

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Literature Corpus work
3aa7ba49-01c0-57a7-8711-916b5e76ea2f
DOI
10.1101/780320
Open publication

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CRISPR-Cas9 generated Pompe knock-in murine model exhibits early-onset hypertrophic cardiomyopathy and skeletal muscle weaknessDOI 10.1101/780320
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