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Autosomal Dominant Nonsyndromic Deafness 82
An autosomal dominant nonsyndromic deafness characterized by onset of rapidly progressive bilateral sensorineural hearing loss usually early in the first decade that is caused by heterozygous mutation in the ATP2B2 gene
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Overview
An autosomal dominant nonsyndromic deafness characterized by onset of rapidly progressive bilateral sensorineural hearing loss usually early in the first decade that is caused by heterozygous mutation in the ATP2B2 gene
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