ID   GM09405
AC   CVCL_UR82
DR   Coriell; GM09405
DR   Wikidata; Q93803387
RX   CelloPub=CLPUB00447;
RX   PubMed=9247083;
CC   Discontinued: Coriell; GM09405; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C85861; Neuronal ceroid lipofuscinosis type 1
DI   ORDO; Orphanet_228329; CLN1 disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   16Y
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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   PubMed=9247083; DOI=10.1016/S0925-4439(97)00033-1;
RA   Verkruyse L.A., Natowicz M.R., Hofmann S.L.;
RT   "Palmitoyl-protein thioesterase deficiency in fibroblasts of
RT   individuals with infantile neuronal ceroid lipofuscinosis and I-cell
RT   disease.";
RL   Biochim. Biophys. Acta 1361:1-5(1997).
//