ID   GM01865
AC   CVCL_DE31
SY   GM-1865; GM1865
DR   Coriell; GM01865
DR   Wikidata; Q54837141
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=7565859;
CC   Discontinued: Coriell; GM01865; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C9460; Cockayne syndrome
DI   ORDO; Orphanet_191; Cockayne syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex ambiguous
AG   36Y
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 8
//
RX   PubMed=7565859; DOI=10.1016/0921-8777(95)00015-C;
RA   Volpe, John P.G.
RA   Cleaver, James Edward
RT   "Xeroderma pigmentosum variant cells are resistant to
RT   immortalization.";
RL   Mutat. Res. 337:111-117(1995).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell, Lewis Lemon
RA   Greene, Arthur 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).
//