ID   GM04196
AC   CVCL_1H91
DR   CLO; CLO_0019503
DR   Coriell; GM04196
DR   Wikidata; Q54838409
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_1H92 ! GM04197
SX   Female
AG   51Y
CA   Finite cell line
DT   Created: 08-07-15; Last updated: 29-06-23; Version: 9
//
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   PubMed=6316146; DOI=10.1038/306234a0;
RA   Gusella, James Francis
RA   Wexler, Nancy Sabin
RA   Conneally, Patrick Michael
RA   Naylor, Susan L.
RA   Anderson, Mary Anne
RA   Tanzi, Rudolph Emile
RA   Watkins, Paul C.
RA   Ottina, Kathleen
RA   Wallace, Margaret R.
RA   Sakaguchi, Alan Y.
RA   Young, Anne Buckingham
RA   Shoulson, Ira
RA   Bonilla, Ernesto
RA   Martin, Joseph Boyd
RT   "A polymorphic DNA marker genetically linked to Huntington's
RT   disease.";
RL   Nature 306:234-238(1983).
//