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Autosomal Dominant Nonsyndromic Deafness 88
An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that is caused by heterozygous mutation in the EPHA10 gene on chromosome 1p34.
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When to seek help
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Overview
An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that is caused by heterozygous mutation in the EPHA10 gene on chromosome 1p34.
Resources
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