ID   GM00470
AC   CVCL_M921
SY   GM-470; GM 470; GM17062
DR   CLO; CLO_0014561
DR   CLO; CLO_0025971
DR   Coriell; GM00470
DR   Coriell; GM17062
DR   Wikidata; Q54836246
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=817596;
RX   PubMed=3017984;
CC   Part of: Human variation panel.
CC   Population: Mexican.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C85052; Sandhoff disease
DI   ORDO; Orphanet_796; Sandhoff disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   1Y
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 29-06-23; Version: 13
//
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=817596;
RA   Rattazzi M.C., Brown J.A., Davidson R.G., Shows T.B.;
RT   "Studies on complementation of beta hexosaminidase deficiency in human
RT   GM2 gangliosidosis.";
RL   Am. J. Hum. Genet. 28:143-154(1976).
//
RX   PubMed=3017984; DOI=10.1016/S0021-9258(18)67145-5;
RA   O'Dowd B.F., Klavins M.H., Willard H.F., Gravel R.A., Lowden J.A.,
RA   Mahuran D.J.;
RT   "Molecular heterogeneity in the infantile and juvenile forms of
RT   Sandhoff disease (O-variant GM2 gangliosidosis).";
RL   J. Biol. Chem. 261:12680-12685(1986).
//