Cellosaurus WG0098 (CVCL_B3WC)
| Cell line name | WG0098 |
|---|---|
| Synonyms | WG98 |
| Accession | CVCL_B3WC |
| Resource Identification Initiative | To cite this cell line use: WG0098 (RRID:CVCL_B3WC) |
| 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 | Sandhoff disease (NCIt: C85052) Sandhoff disease (ORDO: Orphanet_796) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Category | Finite cell line |
| Publications | PubMed=908752; DOI=10.1172/JCI108860; PMCID=PMC372461 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q110433977 |
| Entry history | |
| Entry creation | 16-Dec-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |