ID   CHWi001-A
AC   CVCL_YN68
SY   iPSC31-2; IPS31-2
DR   BioSamples; SAMEA6611121
DR   hPSCreg; CHWi001-A
DR   SKIP; SKIP005795
DR   Wikidata; Q93453419
RX   PubMed=32388443;
CC   From: Center of Prenatal Diagnosis, The Central Hospital of Wenzhou; Wenzhou; China.
CC   Population: Chinese; Han.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C84392; Mental retardation
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   15Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 29-06-23; Version: 6
//
RX   PubMed=32388443; DOI=10.1016/j.scr.2020.101811;
RA   Wan R., Zhang Q., Li H.-Z., Xu X.-Q., Tang S.-H.;
RT   "Generation of an iPSC line (CHWi001-A) from peripheral blood
RT   mononuclear cells in a patient with intellectual disability and
RT   haploinsufficiency of PLPPR4.";
RL   Stem Cell Res. 45:101811-101811(2020).
//