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Autosomal Dominant Nonsyndromic Deafness 28
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and is caused by mutation in the GRHL2 gene on chromosome 8q22.
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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 GRHL2 gene on chromosome 8q22.
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