ID   AG03675
AC   CVCL_A2PE
SY   AG3675
DR   Coriell; AG03675
DR   Wikidata; Q105506232
RX   CelloPub=CLPUB00387;
CC   Discontinued: Coriell; AG03675; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C85028; Progressive supranuclear palsy
DI   ORDO; Orphanet_683; Progressive supranuclear palsy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_A2MF ! AG03674
OI   CVCL_A2MG ! AG03678
SX   Male
AG   60Y
CA   Finite cell line
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 5
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.A.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 7th edition. October 1980.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//