ID   GM00093
AC   CVCL_CW96
SY   GM-93
DR   Coriell; GM00093
DR   Wikidata; Q54836032
RX   DOI=10.5962/bhl.title.4090;
CC   Population: Caucasian.
CC   Discontinued: Coriell; GM00093; probable.
CC   Derived from site: In situ; Umbilical cord; UBERON=UBERON_0002331.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C129932; Nephropathic cystinosis
DI   ORDO; Orphanet_411629; Nephropathic infantile cystinosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_H959 ! GM00090
OI   CVCL_H960 ! GM00304
SX   Male
AG   24FW
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 10
//
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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//