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  • Molecular assay reagents intended to identify deletions or duplications of the ATP binding cassette subfamily A member 4 (ABCA4) gene, located at chromosome 1p22, which encodes the protein retinal-specific ATP-binding cassette transporter. Genetic variants at this locus have been associated with age-related macular degeneration 2, retinitis pigmentosa 19, Stargardt disease 1, and cone-rod dystrophy 3.
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