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Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy.

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第一作者： Kenji Rowel Q,Lim

第一单位： Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, 8812-112 St., Edmonton, AB T6G 2H7, Canada. kenjirow@ualberta.ca.

作者： Kenji Rowel Q,Lim ^[1] ; Chantal,Yoon ^[2] ; Toshifumi,Yokota ^[3]

作者单位： Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, 8812-112 St., Edmonton, AB T6G 2H7, Canada. kenjirow@ualberta.ca. ^[1] Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, 8812-112 St., Edmonton, AB T6G 2H7, Canada. cyoon@ualberta.ca. ^[2] Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, 8812-112 St., Edmonton, AB T6G 2H7, Canada. toshifum@ualberta.ca.;The Friends of Garret Cumming Research and Muscular Dystrophy Canada HM Toupin Neurological Science Research Chair, 8812-112 St., Edmonton, AB T6G 2H7, Canada. toshifum@ualberta.ca. ^[3]

关键词 CRISPR/Cas9 Duchenne muscular dystrophy (DMD)deltaE50-MD dog model exon skipping therapy gene editing human induced pluripotent stem cells (hiPSCs)humanized dystrophic mouse models immortalized patient muscle cells mdx mice

DOI 10.3390/jpm8040038

PMID 30477208

发布时间 2020-10-01

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Journal of personalized medicine

2018年8卷4期

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Journal of personalized medicine

2018年8卷4期

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Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy.

Journal of personalized medicine

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Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy.

Journal of personalized medicine

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Journal of personalized medicine

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