ID   GM00572
AC   CVCL_1K49
SY   GM-572; GM 0572; GM572
DR   CLO; CLO_0026015
DR   Coriell; GM00572
DR   Wikidata; Q54836312
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=6220706;
CC   Population: Caucasian.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C84737; Glycogen storage disease type IV
DI   ORDO; Orphanet_367; Glycogen storage disease due to glycogen branching enzyme deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   2Y
CA   Finite cell line
DT   Created: 08-07-15; 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).
//
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=6220706; DOI=10.1016/0006-291x(83)90354-6;
RA   Brown D.H., Brown B.I.;
RT   "Studies of the residual glycogen branching enzyme activity present in
RT   human skin fibroblasts from patients with type IV glycogen storage
RT   disease.";
RL   Biochem. Biophys. Res. Commun. 111:636-643(1983).
//