ID   GM04799
AC   CVCL_Y887
SY   GM 4799
DR   CLO; CLO_0018270
DR   Coriell; GM04799
DR   Wikidata; Q54838693
RX   CelloPub=CLPUB00447;
RX   PubMed=6230415;
CC   Part of: Venezuelan Huntington disease kindreds subcollection.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_Y886 ! GM04798
SX   Male
AG   47Y
CA   Finite cell line
DT   Created: 10-04-15; Last updated: 29-06-23; Version: 11
//
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=6230415; DOI=10.1016/0022-510x(83)90187-9;
RA   Sumbilla C., Lakowicz J.R.;
RT   "Evidence for normal fibroblast cell membranes from individuals with
RT   Huntington's disease. A fluorescence probe study.";
RL   J. Neurol. Sci. 62:23-40(1983).
//