ID   pWS88-c15
AC   CVCL_RI78
DR   SKIP; SKIP001251
DR   Wikidata; Q54948740
RX   PubMed=27509850;
CC   Omics: Variations; SNP array analysis.
CC   Donor information: Established from a patient that harbors a partial deletion in the WBS critical region.
CC   Derived from site: In situ; Tooth, dental pulp; UBERON=UBERON_0001754.
DI   NCIt; C85232; Williams syndrome
DI   ORDO; Orphanet_904; Williams syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_RI75 ! pWS88-c0
OI   CVCL_RI76 ! pWS88-c1
OI   CVCL_RI77 ! pWS88-c2
OI   CVCL_RI79 ! pWS88-c18
SX   Male
AG   14Y9M
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 10-04-25; Version: 8
//
RX   PubMed=27509850; DOI=10.1038/nature19067; PMCID=PMC4995142;
RA   Chailangkarn T., Trujillo C.A., Freitas B.C., Hrvoj-Mihic B.,
RA   Herai R.H., Yu D.X., Brown T.T., Marchetto M.C.N., Bardy C., McHenry L.,
RA   Stefanacci L., Jarvinen A.M., Searcy Y.M., DeWitt M., Wong W., Lai P.,
RA   Ard M.C., Hanson K.L., Romero S., Jacobs B., Dale A.M., Dai L.,
RA   Korenberg J.R., Gage F.H., Bellugi U., Halgren E., Semendeferi K.,
RA   Muotri A.R.;
RT   "A human neurodevelopmental model for Williams syndrome.";
RL   Nature 536:338-343(2016).
//