ID   GM06056
AC   CVCL_V822
SY   GM6056
DR   CLO; CLO_0023540
DR   Coriell; GM06056
DR   Wikidata; Q54842140
RX   CelloPub=CLPUB00447;
RX   PubMed=6705569;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C85040; Pyruvate carboxylase deficiency
DI   ORDO; Orphanet_3008; Pyruvate carboxylase deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   4M
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 10
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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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   PubMed=6705569; DOI=10.1159/000132035;
RA   Oizumi J., Donnell G.N., Ng W.G., Mulivor R.A., Greene A.E.,
RA   Coriell L.L.;
RT   "Congenital lactic acidosis associated with pyruvate carboxylase
RT   deficiency. Repository identification No. GM6056.";
RL   Cytogenet. Cell Genet. 38:80-80(1984).
//