Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice.
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ABSTRACT:
SUBMITTER: Gu X
PROVIDER: S-EPMC9253335 | biostudies-literature | 2022 Jul
REPOSITORIES: biostudies-literature
Publications
Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice.
Gu Xi X Hu Xinde X Wang Daqi D Xu Zhijiao Z Wang Fang F Li Di D Li Geng-Lin GL Yang Hui H Yang Hui H Li Huawei H Zuo Erwei E Shu Yilai Y
Cell research 20220223 7
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