ID   WS17-c2
AC   CVCL_RI93
DR   SKIP; SKIP001236
DR   Wikidata; Q54994422
RX   PubMed=27509850;
CC   Omics: Transcriptomics; RNAseq.
CC   Omics: Variations; SNP array analysis.
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_RI92 ! WS17-c1
OI   CVCL_RI94 ! WS17-c4
SX   Male
AG   9Y8M
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 10-04-25; Version: 7
//
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).
//