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Autosomal Dominant Nonsyndromic Deafness 36
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and is caused by mutation in the TMC1 gene on chromosome 9q21.
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When to seek help
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Overview
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and is caused by mutation in the TMC1 gene on chromosome 9q21.
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