ID   GM01609
AC   CVCL_JB87
SY   GM-1609
DR   Coriell; GM01609
DR   Wikidata; Q54836945
RX   DOI=10.5962/bhl.title.4090;
CC   Discontinued: Coriell; GM01609; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C35133; Wolfram syndrome
DI   ORDO; Orphanet_3463; Wolfram syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_1D29 ! GM01799
SX   Female
AG   18Y
CA   Finite cell line
DT   Created: 15-05-17; Last updated: 29-06-23; Version: 7
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//