Generation of the human induced pluripotent stem cell line (UKWNLi001-A) from skin fibroblasts of a woman with Fabry disease carrying the X-chromosomal heterozygous c.708 G > C (W236C) missense mutation in exon 5 of the alpha-galactosidase-A gene

Resource table.Unique stem cell line identifierUKWNLi001-AAlternative name(s) of stem cell lineFD-W236C-iPSCInstitutionDepartment of Neurology, University of Würzburg, GermanyContact information of distributorNurcan Üçeyler, ueceyler_n@ukw.deType of cell lineiPSCOriginHumanAdditional origin infoAge: 25Sex: femaleEthnicity: caucasianCell SourceDermal fibroblastsClonalityClonalMethod of reprogrammingmRNA reprogrammingGenetic ModificationN/AType of ModificationN/AAssociated diseaseFabry disease (FD)Gene/locusAlpha-galactosidase A (GLA); Xq22.1c.708 G > CMethod of modificationN/AName of transgene or resistanceN/AInducible/constitutive systemN/ADate archived/stock date05/2017Cell line repository/bankN/AEthical approvalEthics Committee of the University of Würzburg Medical Faculty (#135/15)