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  • Molecular assay reagents intended to identify gene variants associated with Alport syndrome, a heritable disorder affecting kidney function as well as hearing loss and abnormalities of the eyes. Genetic variants at multiple loci have been associated with Alport syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Alport syndrome-associated loci simultaneously.
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