ID   GIBHi001-A
AC   CVCL_XJ81
SY   ASD-hiPSC
DR   BioSamples; SAMEA5928136
DR   hPSCreg; GIBHi001-A
DR   SKIP; SKIP005559
DR   Wikidata; Q93561133
RX   PubMed=31520889;
CC   From: Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences; Guangzhou; China.
CC   Sequence variation: Mutation; HGNC; 3614; FCGR1BP; Simple; p.Arg139Ter (c.415C>T); Zygosity=Heterozygous (PubMed=31520889).
CC   Derived from site: In situ; Urine; UBERON=UBERON_0001088.
DI   NCIt; C88412; Autism spectrum disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   16Y
CA   Induced pluripotent stem cell
DT   Created: 19-12-19; Last updated: 29-06-23; Version: 7
//
RX   PubMed=31520889; DOI=10.1016/j.scr.2019.101571;
RA   Li S., Zhao H.-F., Huang R.-Q., He L., Tian C., Huang H.-L.,
RA   Han X.-B., Tang F., Lin Z.-X., Deng S.-H., Zhou J.-D., Li Z.-Y.;
RT   "Generation of iPSC line (GIBHi001-A) from a patient with autism
RT   spectrum disorder.";
RL   Stem Cell Res. 40:101571-101571(2019).
//