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DEAFNESS, AUTOSOMAL DOMINANT 4B

Known as: DFNA4B 
 
National Institutes of Health

Papers overview

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Review
2020
Review
2020
Over the past decade, advancements in high-throughput sequencing have greatly enhanced our knowledge of the mutational signatures… Expand
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2015
2015
Mutations in CEACAM16 cause autosomal dominant nonsyndromic hearing loss (DFNA4B). So far, 2 families have been reported with… Expand
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