ID   KSCBi007-A
AC   CVCL_WR19
SY   KNIH-PWS001i-A
DR   BioSamples; SAMEA5727775
DR   hPSCreg; KSCBi007-A
DR   SKIP; SKIP005590
DR   Wikidata; Q95980261
RX   PubMed=31756696;
CC   From: National Institute of Health, Korea-National Stem Cell Bank (KSCB); Cheongwon-gun; South Korea.
CC   Population: Asian.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   5M
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 29-06-23; Version: 9
//
RX   PubMed=31756696; DOI=10.1016/j.scr.2019.101647;
RA   Kim B.-Y., Lee J.-S., Kim Y.-O., Park M.-H., Koo S.K.;
RT   "Generation of patient-specific induced pluripotent stem cells
RT   (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain
RT   maternal uniparental disomy (UPD).";
RL   Stem Cell Res. 41:101647-101647(2019).
//