ID   WG0107
AC   CVCL_B3WA
SY   WG107
DR   Wikidata; Q110433980
RX   PubMed=3375249;
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Population: Caucasian; French Canadian.
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C85184; Tay-Sachs disease
DI   ORDO; Orphanet_845; Tay-Sachs disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 16-12-21; Last updated: 29-06-23; Version: 4
//
RX   PubMed=3375249; DOI=10.1073/pnas.85.11.3955; PMCID=PMC280339;
RA   Myerowitz, Rachel
RT   "Splice junction mutation in some Ashkenazi Jews with Tay-Sachs
RT   disease: evidence against a single defect within this ethnic group.";
RL   Proc. Natl. Acad. Sci. U.S.A. 85:3955-3959(1988).
//