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  • Molecular assay reagents intended to identify mutations in the Fanconi anemia complementation group A (FANCA) gene, located at chromosome 16q24.3, which encodes for a protein that functions in the Fanconi anemia core complex, in interstrand DNA cross-link repair, and in the maintenance of normal chromosome stability. Mutations at this locus have been identified in patients with Fanconi anemia (FA).
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