ID   WG1586
AC   CVCL_QZ06
SY   WG 1586
DR   Wikidata; Q54993888
RX   PubMed=7909321;
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; C142172; Methylmalonic aciduria, cblB type
DI   ORDO; Orphanet_79311; Vitamin B12-responsive methylmalonic acidemia type cblB
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   7M
CA   Finite cell line
DT   Created: 05-03-18; Last updated: 29-06-23; Version: 8
//
RX   PubMed=7909321; DOI=10.1172/JCI117166; PMCID=PMC294249;
RA   Qureshi A.A., Crane A.M., Matiaszuk N.V., Rezvani I., Ledley F.D.,
RA   Rosenblatt D.S.;
RT   "Cloning and expression of mutations demonstrating intragenic
RT   complementation in mut0 methylmalonic aciduria.";
RL   J. Clin. Invest. 93:1812-1819(1994).
//