ID   PSMi008-A
AC   CVCL_WJ38
SY   SA2.3-iPS
DR   hPSCreg; PSMi008-A
DR   Wikidata; Q98128688
RX   PubMed=31398660;
CC   From: Institution Fondazione IRCCS Policlinico San Matteo; Pavia; Italy.
CC   Sequence variation: Mutation; HGNC; 16859; NOS1AP; Simple; chr1:g.162065484T>C (g.694T>C); dbSNP=rs16847548; Zygosity=Heterozygous (PubMed=31398660).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   52Y
CA   Induced pluripotent stem cell
DT   Created: 24-05-19; Last updated: 30-01-24; Version: 9
//
RX   PubMed=31398660; DOI=10.1016/j.scr.2019.101510;
RA   Mura M., Pisano F., Stefanello M., Ginevrino M., Boni M., Calabro F.,
RA   Crotti L., Valente E.M., Schwartz P.J., Brink P.A., Gnecchi M.;
RT   "Generation of two human induced pluripotent stem cell (hiPSC) lines
RT   from a long QT syndrome South African founder population.";
RL   Stem Cell Res. 39:101510-101510(2019).
//