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Autosomal Dominant Nonsyndromic Deafness 44
An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and is caused by mutation in the CCDC50 gene on chromosome 3q28.
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Overview
An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and is caused by mutation in the CCDC50 gene on chromosome 3q28.
Resources
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