ID   TUR90010
AC   CVCL_VI18
DR   Wikidata; Q54973377
RX   PubMed=10606667;
CC   Population: Turkish.
CC   Sequence variation: Mutation; HGNC; 12791; WRN; Simple; p.Gln1165Ter (c.3493C>T); ClinVar=VCV000005445; Zygosity=Homozygous (PubMed=10606667).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Transformed cell line
DT   Created: 14-05-18; Last updated: 29-06-23; Version: 9
//
RX   PubMed=10606667; DOI=10.1093/nar/28.2.648;
RA   Moser M.J., Kamath-Loeb A.S., Jacob J.E., Bennett S.E., Oshima J.,
RA   Monnat R.J. Jr.;
RT   "WRN helicase expression in Werner syndrome cell lines.";
RL   Nucleic Acids Res. 28:648-654(2000).
//