ID   KSCBi009-A
AC   CVCL_WR21
SY   KNIH-PWS003i-A
DR   BioSamples; SAMEA5727777
DR   hPSCreg; KSCBi009-A
DR   SKIP; SKIP005770
DR   Wikidata; Q95980263
RX   PubMed=32474395;
CC   From: National Institute of Health, Korea-National Stem Cell Bank (KSCB); Cheongwon-gun; South Korea.
CC   Population: Korean.
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   Male
AG   13Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 29-06-23; Version: 6
//
RX   PubMed=32474395; DOI=10.1016/j.scr.2020.101847;
RA   Kim B.-Y., Lee J.-S., Kim Y.-O., Koo S.K., Park M.-H.;
RT   "Generation of induced pluripotent stem cells (KSCBi009-A) from a
RT   patient with Prader-Willi syndrome (PWS) featuring deletion of the
RT   paternal chromosome region 15q11.2-q13.";
RL   Stem Cell Res. 46:101847-101847(2020).
//