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Autosomal Recessive Nonsyndromic Deafness 32
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that is caused by mutation in the CDC14A gene
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that is caused by mutation in the CDC14A gene
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