ID   GM00963
AC   CVCL_1V22
SY   GM-963
DR   CLO; CLO_0029506
DR   Coriell; GM00963
DR   Wikidata; Q54836567
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=30052969;
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C122782; Hurler-Scheie syndrome
DI   ORDO; Orphanet_93476; Hurler-Scheie syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   5Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 9
CH   CVCL_B5TK ! HT147D
//
RX   PubMed=30052969; DOI=10.1093/hmg/ddy259; PMCID=PMC6454448;
RA   Swaroop, Manju
RA   Brooks, Matthew J.
RA   Gieser, Linn
RA   Swaroop, Anand
RA   Zheng, Wei
RT   "Patient iPSC-derived neural stem cells exhibit phenotypes in
RT   concordance with the clinical severity of mucopolysaccharidosis I.";
RL   Hum. Mol. Genet. 27:3612-3626(2018).
//
RX   CelloPub=CLPUB00447;
RA   Mulivor, Richard A.
RA   Suchy, Sharon 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).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell, Lewis Lemon
RA   Greene, Arthur 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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//