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Molecular assay reagents intended to identify mutations in genes associated with nonsyndromic hearing loss and deafness, a collection of genetic hearing loss and deafness diseases that are not associated with signs and symptoms affecting other parts of the body. Genetic variants at multiple loci have been associated with nonsyndromic hearing loss and deafness. These reagents are intended to detect mutations in multiple nonsyndromic hearing loss/deafness-associated loci simultaneously.
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