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Autosomal Recessive Nonsyndromic Deafness 30
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutations in the MYO3A gene on chromosome 10p12.1.
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutations in the MYO3A gene on chromosome 10p12.1.
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