ID   AS iPS del 1-1
AC   CVCL_U499
SY   ASdel1-1
DR   Wikidata; Q54750575
RX   PubMed=20876107;
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C75462; Angelman syndrome
DI   ORDO; Orphanet_72; Angelman syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_U498 ! AS iPS del 1-0
SX   Female
CA   Induced pluripotent stem cell
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 9
//
RX   PubMed=20876107; DOI=10.1073/pnas.1004487107;
RA   Chamberlain S.J., Chen I.P.-F., Ng K.Y., Bourgois-Rocha F.,
RA   Lemtiri-Chlieh F., Levine E.S., Lalande M.;
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).
//