ID   WS79-c3
AC   CVCL_RJ02
DR   SKIP; SKIP001246
DR   Wikidata; Q54994439
RX   PubMed=27509850;
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_RJ01 ! WS79-c2
OI   CVCL_RJ03 ! WS79-c5
SX   Male
AG   13Y6M
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 29-06-23; Version: 6
//
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).
//