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  • Molecular assay reagents intended to identify mutations in the Fanconi anemia, complementation group F (FANCF) gene, located at chromosome 11p15, which encodes for a DNA repair protein that may operate in a postreplication repair or cell cycle checkpoint function and may also be implicated 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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