Cellosaurus WG0738 (CVCL_UH69)
Cell line name | WG0738 |
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Synonyms | WG 738 |
Accession | CVCL_UH69 |
Resource Identification Initiative | To cite this cell line use: WG0738 (RRID:CVCL_UH69) |
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) |
Sex of cell | Female |
Age at sampling | 6M |
Category | Finite cell line |
Publications | CLPUB00452 PubMed=3937470; DOI=10.1111/j.1749-6632.1985.tb14891.x |
Cross-references | |
Encyclopedic resources | Wikidata; Q98134860 |
Entry history | |
Entry creation | 25-Feb-2019 |
Last entry update | 29-Jun-2023 |
Version number | 7 |