The gene therapy for corneal pathology with novel nonsense cystinosis mouse lines created by CRISPR Gene Editing.
The gene therapy for corneal pathology with novel nonsense cystinosis mouse lines created by CRISPR Gene Editing.
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利用 CRISPR 基因编辑创建的新型无意义胱氨酸病小鼠品系进行角膜病理基因治疗。
DOI：
10.1016/j.jtos.2023.06.002
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发表时间：
2023
期刊：
影响因子：
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通讯作者：
Kao,WinstonW-Y
中科院分区：
文献类型：
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作者：
Dong,Fei;Amlal,Hassane;Venkatakrishnan,Jhuwala;Zhang,Jianhua;Fry,Matthew;Yuan,Yong;Cheng,YuChia;Hu,Yueh-Chiang;Kao,WinstonW-Y
