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Cellosaurus WG3412 (CVCL_B4F1)

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Cell line name WG3412
Accession CVCL_B4F1
Resource Identification Initiative To cite this cell line use: WG3412 (RRID:CVCL_B4F1)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Arakawa syndrome II (NCIt: C99081)
Methylcobalamin deficiency type cblG (ORDO: Orphanet_2170)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=19058814; DOI=10.1016/j.jpeds.2008.10.043
Isabelle Racine Miousse, David Watkins, David Coelho, Tony Rupar, Eric Albert Crombez, Eric Vilain, Jonathan A. Bernstein, Tina Cowan, Christopher Lee-Messer, Gregory M. Enns, Brian Fowler, David S. Rosenblatt;
Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
J. Pediatr. 154:551-556(2009)

Cross-references
Encyclopedic resources Wikidata; Q110434318
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4