ID   WG0699
AC   CVCL_UH68
SY   WG 699
DR   Wikidata; Q98134854
RX   CelloPub=CLPUB00452;
RX   PubMed=3937470;
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C156424; Hereditary folate malabsorption
DI   ORDO; Orphanet_90045; Hereditary folate malabsorption
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   40Y
CA   Finite cell line
DT   Created: 25-02-19; Last updated: 29-06-23; Version: 7
//
RX   CelloPub=CLPUB00452;
RA   Buchanan J.A.;
RT   "Fibroblast plasma membrane vesicles to study inborn errors of
RT   transport.";
RL   Thesis PhD (1984); McGill University Montreal; Montreal; Canada.
//
RX   PubMed=3937470; DOI=10.1111/j.1749-6632.1985.tb14891.x;
RA   Buchanan J.A., Rosenblatt D.S., Scriver C.R.;
RT   "Cultured human fibroblasts and plasma membrane vesicles to
RT   investigate transport function and the effects of genetic mutation.";
RL   Ann. N. Y. Acad. Sci. 456:401-403(1985).
//