ID   GM01125
AC   CVCL_DF15
SY   GM-1125
DR   CLO; CLO_0030166
DR   BioSample; SAMN00803642
DR   Coriell; GM01125
DR   Wikidata; Q54836654
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
CC   Derived from site: In situ; Eye, cornea; UBERON=UBERON_0000964.
DI   NCIt; C168999; Macular dystrophy, retinal, 1
DI   ORDO; Orphanet_75327; North Carolina macular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   41Y
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 8
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
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).
//