ID   GM10625
AC   CVCL_DD85
DR   CLO; CLO_0024548
DR   BioSample; SAMN00800109
DR   Coriell; GM10625
DR   Wikidata; Q54844561
RX   CelloPub=CLPUB00447;
CC   Population: Jewish.
CC   Derived from site: In situ; Buttock, skin; UBERON=UBERON_8480014.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C34864; Hereditary optic atrophy
DI   ORDO; Orphanet_98671; Hereditary optic neuropathy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_DD84 ! GM10624
SX   Male
AG   50Y
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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//