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A generation of human-induced pluripotent stem cell line (MUi032-A) from a Choroideremia disease patient carrying a hemizygous mutation on the CHM gene.

Stem cell research - 1 Dec 2022

Pongpaksupasin Phitchapa, Wongkummool Wasinee, Tong-Ngam Pirut, Jearawiriyapaisarn Natee, Paiboonsukwong Kittiphong, Sangkitporn Siripakorn, Trinavarat Adisak, Atchaneeyasakul La-Ongsri, Tubsuwan Alisa

Abstract excerpt

Choroideremia (CHM) is a monogenic, X-linked inherited retinal disease caused by mutations in the CHM gene. CHM patients develop progressive loss of vision due to degeneration of cell layers in the retina. In this report, the human-induced pluripotent stem cell, MUi032-A, was generated from CD34+ hematopoietic stem/progenitor cells of a male CHM patient by co-electroporation of non-integration episomal vectors...

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Identifiers

PMID: 36395688
DOI: 10.1016/j.scr.2022.102964

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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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