ID   GM00243
AC   CVCL_6B35
SY   GM-243; GM 243
DR   CLO; CLO_0025492
DR   Coriell; GM00243
DR   Wikidata; Q54836111
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=2864994;
CC   Population: Caucasian.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C61251; Metachromatic leukodystrophy
DI   ORDO; Orphanet_512; Metachromatic leukodystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   3Y6M
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 9
//
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=2864994; DOI=10.1017/S0317167100047168;
RA   Farrell K., Applegarth D.A., Toone J.R., McLeod P.M., Savage A.V.;
RT   "Pseudoarylsulfatase-A deficiency in the neurologically impaired
RT   patient.";
RL   Can. J. Neurol. Sci. 12:274-277(1985).
//