ID   NUIGi022-A
AC   CVCL_WT08
SY   ND11C2
DR   BioSamples; SAMEA5780091
DR   hPSCreg; NUIGi022-A
RX   PubMed=31759289;
CC   From: National University of Ireland Galway; Galway; Ireland.
CC   Population: Caucasian.
CC   Sequence variation: Heterozygous for NRXN1 Ex1-5del (PubMed=31759289).
CC   Derived from sampling site: Skin.
DI   NCIt; C88412; Autism spectrum disorder
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_XI98 ! NUIGi022-B
SX   Male
AG   14Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 19-12-19; Version: 3
//
RX   PubMed=31759289; DOI=10.1016/j.scr.2019.101653;
RA   Ding Y.-C., Marco de la Cruz B., Xia Y.-W., Liu M., Lu Y., McInerney V.,
RA   Krawczyk J., Lynch S.A., Howard L., O'Brien T., Gallagher L.,
RA   Shen S.-B.;
RT   "Derivation of familial iPSC lines from three ASD patients carrying
RT   NRXN1alpha(+/-) and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A,
RT   NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B;
RT   NUIGi026-A, NUIGi026-B).";
RL   Stem Cell Res. 41:101653-101653(2019).
//