Cellosaurus WG0738 (CVCL_UH69)
| Cell line name | WG0738 |
|---|---|
| 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 |