ID   NUIGi041-B
SY   ND3C4
DR   BioSamples; SAMEA6465064
DR   hPSCreg; NUIGi041-B
DR   Wikidata; Q98128212
RX   PubMed=33578364;
CC   From: National University of Ireland Galway; Galway; Ireland.
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 8008; NRXN1; Unexplicit; Ex1-5del; Zygosity=Heterozygous (PubMed=33578364).
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C88412; Autism spectrum disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_YQ98 ! NUIGi041-A
SX   Male
AG   20Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 29-06-23; Version: 6
RX   PubMed=33578364; DOI=10.1016/j.scr.2021.102222;
RA   Ding Y.-C., O'Brien A., de la Cruz B.M., Yang M.-M., Fitzgerald J.,
RA   Yang G.-M., Li W.-D., McInerney V., Krawczyk J., Lynch S.A., Howard L.,
RA   Allen N.M., O'Brien T., Gallagher L., Shen S.-B.;
RT   "Derivation of iPSC lines from two patients with autism spectrum
RT   disorder carrying NRXN1alpha deletion (NUIGi041-A, NUIG041-B;
RT   NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B).";
RL   Stem Cell Res. 52:102222-102222(2021).