ID   WG1663
AC   CVCL_QZ32
DR   Wikidata; Q54993914
RX   PubMed=1627355;
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Miscellaneous: Cell line no longer available.
CC   Misspelling: WB1663; PubMed=1627355.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C142173; Homocystinuria-megaloblastic anemia, cblE complementation type
DI   ORDO; Orphanet_2169; Methylcobalamin deficiency type cblE
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 05-03-18; Last updated: 29-06-23; Version: 7
//
RX   PubMed=1627355; DOI=10.1016/0885-4505(92)90032-T;
RA   Sillaots, Susan Linda
RA   Hall, Charles A.
RA   Hurteloup, Valerie
RA   Rosenblatt, David S.
RT   "Heterogeneity in cblG: differential retention of cobalamin on
RT   methionine synthase.";
RL   Biochem. Med. Metab. Biol. 47:242-249(1992).
//