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  • Molecular assay reagents intended to identify gene variants associated with nonsyndromic hearing loss and deafness, a collection of genetic hearing loss and deafness disorders 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 various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple nonsyndromic hearing loss and deafness-associated loci simultaneously.
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