Generation of the induced pluripotent stem cell line ISMMSi061-A from a patient with ataxia, intention tremor, and hypotonia syndrome, childhood-onset

Summary

We have described a novel neurodevelopmental disorder caused by de novo, heterozygous pathogenic variants in the Pou domain, class 4, transcription factor 1 (POU4F1), now termed ataxia, intention tremor, and hypotonia syndrome, childhood-onset (ATITHS). This study reports the generation and characterization of an induced pluripotent stem cell (iPSC) line derived from peripheral blood mononuclear cells of a patient with ATITHS. The resulting iPSC line, ISMMSi061-A, harbors the POU4F1 heterozygous variant c.271_281del;p.(Thr91Hisfs*254). The iPSCs display normal cell morphology, expression of pluripotency markers, normal karyotype, and the ability to differentiate into all three germ layers. Copyright © 2026 The Author(s). Published by Elsevier B.V. All rights reserved.

Authors Liu NN, Hu R, Hubbard SJ, Salemi SE, Baljinnyam E, Pradhan P, Smith G, Webb BD, Marro SG
Journal Stem cell research
Publication Date 2026 Apr;92:103938
PubMed 41723941
DOI 10.1016/j.scr.2026.103938

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