ID   PWS SD fibroblast
AC   CVCL_ZJ46
SY   PWS Small atypical Deletion fibroblast
DR   Wikidata; Q98128722
RX   PubMed=24363065;
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   19Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
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RX   PubMed=24363065; DOI=10.1093/hmg/ddt628; PMCID=PMC3976333;
RA   Martins-Taylor K., Hsiao J.S., Chen I.P.-F., Glatt-Deeley H.R.,
RA   De Smith A.J., Blakemore A.I.F., Lalande M.E., Chamberlain S.J.;
RT   "Imprinted expression of UBE3A in non-neuronal cells from a
RT   Prader-Willi syndrome patient with an atypical deletion.";
RL   Hum. Mol. Genet. 23:2364-2373(2014).
//