ID   NUIGi006-B
SY   LQTS005C4; LQT005C4
DR   BioSamples; SAMEA5912493
DR   hPSCreg; NUIGi006-B
RX   PubMed=31415974;
CC   From: National University of Ireland Galway; Galway; Ireland.
CC   Sequence variation: Heterozygous for KCNQ1 p.Ser566Tyr (c.1697C>A) (PubMed=31415974).
DI   NCIt; C85049; Long QT syndrome 1
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_WS90 ! NUIGi006-A
OI   CVCL_WS92 ! NUIGi006-C
SX   Male
AG   40Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 06-09-19; Version: 2
RX   PubMed=31415974; DOI=10.1016/j.scr.2019.101502;
RA   Ge N., Liu M., Krawczyk J., McInerney V., Galvin J., Shen S.,
RA   O'Brien T., Prendiville T.;
RT   "Generation of eight human induced pluripotent stem cell (iPSC) lines
RT   from familial Long QT Syndrome type 1 (LQT1) patients carrying KCNQ1
RT   c.1697C>A mutation (NUIGi005-A, NUIGi005-B, NUIGi005-C, NUIGi006-A,
RT   NUIGi006-B, NUIGi006-C, NUIGi007-A, and NUIGi007-B).";
RL   Stem Cell Res. 39:101502-101502(2019).