| Cell line name | WG2215 |
|---|---|
| Accession | CVCL_UH94 |
| Resource Identification Initiative | To cite this cell line use: WG2215 (RRID:CVCL_UH94) |
| 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 | Holocarboxylase synthetase deficiency (NCIt: C98842) Holocarboxylase synthetase deficiency (ORDO: Orphanet_79242) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Category | Finite cell line |
| Publications | PubMed=16098205; DOI=10.1111/j.1742-4658.2005.04839.x |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q98134913 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |