ID   GM03056
AC   CVCL_U519
SY   GM3056
DR   CLO; CLO_0013504
DR   BioSample; SAMN00808231
DR   Coriell; GM03056
DR   Wikidata; Q54837844
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   PubMed=7174798;
CC   Population: Caucasian.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C150601; Citrullinemia type I
DI   ORDO; Orphanet_247525; Citrullinemia type I
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_U516 ! GM01679
OI   CVCL_U518 ! GM01685
SX   Male
AG   3Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 12
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.A.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 7th edition. October 1980.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//
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   CelloPub=CLPUB00720;
RA   Greene A.E., Mulivor R.A.;
RT   "1986/1987 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 13th edition. October 1986.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (1986).
//
RX   PubMed=7174798; DOI=10.1172/JCI110736;
RA   Su T.-S., Bock H.-G.O., Beaudet A.L., O'Brien W.E.;
RT   "Molecular analysis of argininosuccinate synthetase deficiency in
RT   human fibroblasts.";
RL   J. Clin. Invest. 70:1334-1339(1982).
//