Journal
STEM CELL RESEARCH
Volume 60, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.scr.2022.102738
Keywords
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Funding
- Aviesan-Unadev
- Vaincre Usher 2
- Fondation de France
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We report the generation of a human iPSC line from a patient with autosomal recessive retinitis pigmentosa using the non-integrative Sendai virus method. The generated iPSC line is pluripotent and genetically stable, and will serve as a valuable tool for studying the pathophysiology associated with the disease.
We report here the generation of the human iPSC line INMi005-A from a patient with non-syndromic autosomal recessive retinitis pigmentosa caused by compound heterozygous mutations in the USH2A gene. The reprogramming of primary human dermal fibroblasts was performed using the non-integrative Sendai virus method and the OSKM transcription factor cocktail. The generated INMi005-A iPSC line is pluripotent and genetically stable, and will represent a valuable tool for understanding the pathophysiology associated with USH2A mutations.
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