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Article

Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa.

Stem cell research - 1 Apr 2022

Sanjurjo-Soriano Carla, Erkilic Nejla, Vache Christel, Dubois Gregor, Roux Anne-Françoise, Meunier Isabelle, Kalatzis Vasiliki

Abstract excerpt

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...

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Identifiers

PMID: 35248879
DOI: 10.1016/j.scr.2022.102738

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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