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Molecular assay reagents intended to identify gene variants in the majority of genes known to be associated with hearing loss and deafness. Genetic variants at multiple loci have been associated with hearing loss/deafness. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of hearing loss/deafness-associated loci simultaneously.
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