ID   CHCMUi002-A
AC   CVCL_C9Z7
DR   BioSamples; SAMEA113595353
DR   hPSCreg; CHCMUi002-A
DR   Wikidata; Q123030909
RX   PubMed=38134578;
CC   From: Children's hospital of Chongqing Medical University; Chongqing; China.
CC   Population: Chinese; Han.
CC   Sequence variation: Mutation; HGNC; HGNC:2578; CYBB; Simple; c.785_786delTT; Zygosity=Hemizygous (PubMed=38134578).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C26788; Chronic granulomatous disease
DI   ORDO; Orphanet_379; Chronic granulomatous disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   2Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 19-12-24; Version: 4
//
RX   PubMed=38134578; DOI=10.1016/j.scr.2023.103269;
RA   Zeng A.-L., Ni K., Fang S.-Y., Yu L., Gao Y.-L., Zhou L.-N., Zhao X.-D.;
RT   "Generation of a human iPSC line (CHCMUi002-A) from peripheral blood
RT   mononuclear cells from a chronic granulomatous disease patient.";
RL   Stem Cell Res. 74:103269-103269(2024).
//