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Cellosaurus GM10389 (CVCL_RB00)

[Text version]
Cell line name GM10389
Accession CVCL_RB00
Resource Identification Initiative To cite this cell line use: GM10389 (RRID:CVCL_RB00)
Comments Population: African American.
Cell type: Fibroblast; CL=CL_0000057.
Disease Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 4 (NCIt: C126741)
Congenital muscular dystrophy, Fukuyama type (ORDO: Orphanet_272)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 7Y
Category Finite cell line
Publications

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
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; GM10389
Cell line databases/resources CLO; CLO_0028569
Biological sample resources BioSample; SAMN00799981
Encyclopedic resources Wikidata; Q54844429
Entry history
Entry creation05-Mar-2018
Last entry update29-Jun-2023
Version number7