ID   PWS iPS del 1-7
AC   CVCL_U529
SY   PWS1-7
DR   Kerafast; ECN002
DR   Kerafast; ECN015
DR   SKIP; SKIP005164
DR   Wikidata; Q54948729
RX   PubMed=20876107;
CC   Discontinued: Kerafast; ECN002; true.
CC   Discontinued: Kerafast; ECN015; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_5I47 ! WG1534
SX   Female
CA   Induced pluripotent stem cell
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 14
//
RX   PubMed=20876107; DOI=10.1073/pnas.1004487107; PMCID=PMC2955112;
RA   Chamberlain S.J., Chen I.P.-F., Ng K.Y., Bourgois-Rocha F.,
RA   Lemtiri-Chlieh F., Levine E.S., Lalande M.E.;
RT   "Induced pluripotent stem cell models of the genomic imprinting
RT   disorders Angelman and Prader-Willi syndromes.";
RL   Proc. Natl. Acad. Sci. U.S.A. 107:17668-17673(2010).
//