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DEAFNESS, AUTOSOMAL DOMINANT 4B
National Institutes of Health
Autosomal dominant inheritance
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A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment
Michaela A. H. Hofrichter
Corpus ID: 22518776
Mutations in CEACAM16 cause autosomal dominant nonsyndromic hearing loss (DFNA4B). So far, 2 families have been reported with…
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