ID   HPS2296
AC   CVCL_YS53
SY   BRCi020-A
DR   hPSCreg; BRCi020-A
DR   RCB; HPS2296
DR   Wikidata; Q94220064
RX   PubMed=35292424;
CC   Population: Japanese.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C2989; 22q11.2 deletion syndrome
DI   ORDO; Orphanet_567; 22q11.2 deletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_YS54 ! HPS2297
OI   CVCL_YS55 ! HPS2298
OI   CVCL_YS56 ! HPS2299
OI   CVCL_YS57 ! HPS2300
SX   Male
AG   1-5Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 05-10-23; Version: 6
//
RX   PubMed=35292424; DOI=10.1016/j.scr.2022.102744;
RA   Shimizu T., Matsuo-Takasaki M., Luijkx D., Takami M., Arai Y.,
RA   Noguchi M., Nakamura Y., Hayata T., Saito M.K., Hayashi Y.;
RT   "Generation of human induced pluripotent stem cell lines derived from
RT   four DiGeorge syndrome patients with 22q11.2 deletion.";
RL   Stem Cell Res. 61:102744-102744(2022).
//