ID   GM02935
AC   CVCL_JX70
DR   CLO; CLO_0012828
DR   BioSample; SAMN00808174
DR   Coriell; GM02935
DR   Wikidata; Q54837756
RX   CelloPub=CLPUB00447;
CC   Population: Arab.
CC   Derived from site: In situ; Labioscrotal fold, skin; UBERON=UBERON_8480029.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C98699; 5 alpha steroid reductase 2 deficiency
DI   ORDO; Orphanet_753; 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   16Y
CA   Finite cell line
DT   Created: 22-08-17; Last updated: 29-06-23; Version: 10
//
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).
//