ID   GM01022
AC   CVCL_V790
SY   GM-1022; GM01022A
DR   CLO; CLO_0029494
DR   BioSample; SAMN00803567
DR   Coriell; GM01022
DR   Wikidata; Q54836607
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=806052;
RX   PubMed=826372;
CC   Population: Caucasian.
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C61264; Maroteaux-Lamy syndrome
DI   ORDO; Orphanet_583; Mucopolysaccharidosis type 6
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_V775 ! GM00519
OI   CVCL_V821 ! GM05358
SX   Female
AG   4Y
CA   Transformed cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 14
//
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=806052; DOI=10.1203/00006450-197505000-00003;
RA   Beratis N.G., Turner B.M., Weiss R., Hirschhorn K.;
RT   "Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: cellular
RT   studies and carrier identification.";
RL   Pediatr. Res. 9:475-480(1975).
//
RX   PubMed=826372; DOI=10.1159/000130717;
RA   Beratis N.G., Hirschhorn K., Friedman S., Greene A.E., Coriell L.L.;
RT   "Maroteaux-Lamy syndrome: repository identification Nos. GM-519, 520,
RT   935, 943, and 1022.";
RL   Cytogenet. Cell Genet. 17:236-238(1976).
//