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Cellosaurus WG0103 (CVCL_B3WB)

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Cell line name WG0103
Synonyms WG103
Accession CVCL_B3WB
Resource Identification Initiative To cite this cell line use: WG0103 (RRID:CVCL_B3WB)
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 Tay-Sachs disease (NCIt: C85184)
Tay-Sachs disease (ORDO: Orphanet_845)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=3375249; DOI=10.1073/pnas.85.11.3955; PMCID=PMC280339
Rachel Myerowitz;
Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic group.
Proc. Natl. Acad. Sci. U.S.A. 85:3955-3959(1988)

Cross-references
Encyclopedic resources Wikidata; Q110433978
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4