ID   SJTUXHi002-A
AC   CVCL_C0F7
DR   BioSamples; SAMEA11567037
DR   hPSCreg; SJTUXHi002-A
DR   Wikidata; Q112930397
RX   PubMed=35134694;
CC   From: Shanghai Xinhua Hospital, Shanghai Jiao Tong University; Shanghai; China.
CC   Population: Chinese; Han.
CC   Sequence variation: Mutation; HGNC; 4572; GRIA2; Simple; c.1998delT; Zygosity=Heterozygous (PubMed=35134694).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C88412; Autism spectrum disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   8Y
CA   Induced pluripotent stem cell
DT   Created: 23-06-22; Last updated: 29-06-23; Version: 4
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RX   PubMed=35134694; DOI=10.1016/j.scr.2022.102676;
RA   Ji Y., Lv H., Chen Z.-L., Yu J.-H., Fang S.-F., Li F.;
RT   "Generation of a human induced pluripotent stem cell line
RT   (SJTUXHi002-A) from an individual with autism spectrum disorder
RT   carrying a heterozygous mutation in GRIA2.";
RL   Stem Cell Res. 60:102676-102676(2022).
//