ID   GM11660
AC   CVCL_UR73
DR   Coriell; GM11660
DR   Wikidata; Q93816696
RX   CelloPub=CLPUB00447;
CC   Discontinued: Coriell; GM11660; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C84734; Glycogen storage disease type II
DI   ORDO; Orphanet_365; Glycogen storage disease due to acid maltase deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   30Y
CA   Finite cell line
DT   Created: 25-02-19; Last updated: 29-06-23; Version: 6
//
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).
//