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Cellosaurus GM02095 (CVCL_H178)

[Text version]
Cell line name GM02095
Synonyms GM-2095
Accession CVCL_H178
Resource Identification Initiative To cite this cell line use: GM02095 (RRID:CVCL_H178)
Comments Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Disease Metachromatic leukodystrophy (NCIt: C61251)
Metachromatic leukodystrophy (ORDO: Orphanet_512)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 18FW
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; GM02095
Cell line databases/resources CLO; CLO_0031822
Biological sample resources BioSample; SAMN00807482
Encyclopedic resources Wikidata; Q54837299
Entry history
Entry creation11-Feb-2013
Last entry update29-Jun-2023
Version number12