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Cellosaurus GM00032 (CVCL_0P12)

[Text version]
Cell line name GM00032
Synonyms GM-32
Accession CVCL_0P12
Resource Identification Initiative To cite this cell line use: GM00032 (RRID:CVCL_0P12)
Comments Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Disease Hepatolenticular degeneration (NCIt: C84756)
Wilson disease (ORDO: Orphanet_905)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 9Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM00032
Cell line databases/resources CLO; CLO_0025183
Encyclopedic resources Wikidata; Q54835986
Entry history
Entry creation10-Apr-2015
Last entry update29-Jun-2023
Version number10