ID   GM03390
AC   CVCL_1F14
SY   GM3390
DR   CLO; CLO_0016621
DR   BioSample; SAMN00808385
DR   Coriell; GM03390
DR   Wikidata; Q54838042
RX   CelloPub=CLPUB00447;
RX   PubMed=33329388;
CC   Population: Arab.
CC   Omics: Metabolome analysis.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84736; Glycogen storage disease type III
DI   ORDO; Orphanet_366; Glycogen storage disease due to glycogen debranching enzyme deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y4M
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   PubMed=33329388; DOI=10.3389/fendo.2020.579981;
RA   Hannibal L., Theimer J., Wingert V., Klotz K., Bierschenk I.,
RA   Nitschke R., Spiekerkoetter U., Grunert S.C.;
RT   "Metabolic profiling in human fibroblasts enables subtype clustering
RT   in glycogen storage disease.";
RL   Front. Endocrinol. 11:579981.1-579981.14(2020).
//