Generation of a gene-corrected human iPSC line (CSUASOi004-A-1) from a retinitis pigmentosa patient with heterozygous c.2699 G>A mutation in the PRPF6 gene

Generation of a gene-corrected human iPSC line (CSUASOi004-A-1) from a retinitis pigmentosa patient with heterozygous c.2699 G>A mutation in the PRPF6 gene

Retinitis pigmentosa (RP) is one of the most common inherited retinal diseases characterized by nyctalopia, progressive vision loss and visual field contraction. we previously generated an induced pluripotent stem cell line (CSUASOi004-A) from a RP patient with heterozygous PRPF6 c.2699 G>A (p.R9...

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Bibliographic Details
Main Authors: Yuqin Liang, Xihao Sun, Chunwen Duan, Yalan Zhou, Zekai Cui, Chengcheng Ding, Jianing Gu, Shengru Mao, Shangli Ji, Hon Fai Chan, Shibo Tang, Jiansu Chen
Format: Article
Language:English
Published: Elsevier 2022-10-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506122002604

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http://www.sciencedirect.com/science/article/pii/S1873506122002604

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