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  • Molecular assay reagents intended to identify gene variants associated with retinitis pigmentosa and Leber congenital amaurosis, two related retinopathies that lead to vision loss beginning early in life. Genetic variants at multiple loci have been associated with retinitis pigmentosa and Leber congenital amaurosis. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple retinitis pigmentosa and Leber congenital amaurosis-associated loci simultaneously.
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