Generation of diseased and isogenic control human induced pluripotent stem cell lines MHHi043-A & MHHi043-B from a female Fabry disease patient carrying c.644A > G missense mutation

Summary

Fabry disease (FD) is a monogenic, X-linked lysosomal storage disorder originating from mutations in the GLA gene, which encodes alpha-galactosidase A. Impaired enzyme activity leads to accumulation of the substrate globotriaosylceramide (Gb3) and a multisystemic phenotype. Here, we generated two human induced pluripotent stem cell (hiPSC) lines from a female FD patient carrying a heterozygous c.644A > G missense mutation. The hiPSCs displayed normal karyotype, typical morphology, trilineage differentiation capacity and expressed markers of undifferentiated hPSC state. Consequently, MHHi043-A and MHHi043-B provide a valuable resource for studying FD mechanisms and developing therapeutic strategies. Copyright © 2026 The Author(s). Published by Elsevier B.V. All rights reserved.

Authors Heise N, Borisch C, Jahn C, Sonnenschein K, Donato ND, Gietz A, Buchegger T, Lachmann N, Bär C, Thum T, Hoepfner J, Juchem M
Journal Stem cell research
Publication Date 2026 Aug 17;95:104084
PubMed 42628136
DOI 10.1016/j.scr.2026.104084

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