ID   GM01896
AC   CVCL_F017
SY   GM-1896
DR   CLO; CLO_0032427
DR   BioSample; SAMN00807286
DR   Coriell; GM01896
DR   Wikidata; Q54837167
RX   CelloPub=CLPUB00447;
CC   Population: Caucasian.
CC   Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C61260; Hunter syndrome
DI   ORDO; Orphanet_580; Mucopolysaccharidosis type 2
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   20FW
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 29-06-23; Version: 13
//
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).
//