ID   GM02338
AC   CVCL_D869
SY   GM-2338
DR   CLO; CLO_0033127
DR   BioSample; SAMN00807719
DR   Coriell; GM02338
DR   Wikidata; Q54837439
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=477417;
CC   Population: Caucasian.
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_7356 ! GM02290
OI   CVCL_7357 ! GM02291
OI   CVCL_D868 ! GM02292
SX   Male
AG   15FW
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 29-06-23; Version: 14
//
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).
//
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).
//
RX   PubMed=477417; DOI=10.1159/000131379;
RA   Tischfield J.A., Schafer I.A., Dickerman L.H., Trill J.J., Mulivor R.A.,
RA   Greene A.E., Coriell L.L.;
RT   "Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291,
RT   2292, 2338, 3115, 3116, and 3117.";
RL   Cytogenet. Cell Genet. 24:199-200(1979).
//