ID   WG3728
AC   CVCL_B4F5
DR   Wikidata; Q110434377
RX   PubMed=19058814;
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; C142174; Methylmalonic aciduria and homocystinuria, cblC type
DI   ORDO; Orphanet_79282; Methylmalonic acidemia with homocystinuria, type cblC
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 16-12-21; Last updated: 29-06-23; Version: 4
//
RX   PubMed=19058814; DOI=10.1016/j.jpeds.2008.10.043;
RA   Miousse, Isabelle Racine
RA   Watkins, David
RA   Coelho, David
RA   Rupar, Tony
RA   Crombez, Eric Albert
RA   Vilain, Eric
RA   Bernstein, Jonathan A.
RA   Cowan, Tina
RA   Lee-Messer, Christopher
RA   Enns, Gregory M.
RA   Fowler, Brian
RA   Rosenblatt, David S.
RT   "Clinical and molecular heterogeneity in patients with the cblD inborn
RT   error of cobalamin metabolism.";
RL   J. Pediatr. 154:551-556(2009).
//