ID   GM04212
AC   CVCL_1I02
DR   CLO; CLO_0019516
DR   Coriell; GM04212
DR   Wikidata; Q54838428
RX   CelloPub=CLPUB00447;
RX   PubMed=6316146;
CC   Population: Caucasian.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_1I03 ! GM04213
SX   Female
AG   50Y
CA   Finite cell line
DT   Created: 08-07-15; 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   PubMed=6316146; DOI=10.1038/306234a0;
RA   Gusella J.F., Wexler N.S., Conneally P.M., Naylor S.L., Anderson M.A.,
RA   Tanzi R.E., Watkins P.C., Ottina K., Wallace M.R., Sakaguchi A.Y.,
RA   Young A.B., Shoulson I., Bonilla E., Martin J.B.;
RT   "A polymorphic DNA marker genetically linked to Huntington's
RT   disease.";
RL   Nature 306:234-238(1983).
//