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, deafness, autosomal dominant 48
National Institutes of Health
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A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian family
Corpus ID: 28077750
Non-syndromic hearing loss is the most common sensory disorder in humans; 15%–20% of cases are transmitted as a dominant trait…
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