DEAFNESS, AUTOSOMAL DOMINANT 23
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Background: Non-syndromic hearing loss is among the most genetically heterogeneous traits known in humans. To date, at least 50… Expand Autosomal recessive nonsyndromic deafness is one of the most frequent forms of inherited hearing impairment. Over 30 autosomal… Expand DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss German kindred. DNA samples… Expand