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Autosomal Recessive Nonsyndromic Deafness 59
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutation in the DFNB59 gene on chromosome 2q31.
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When to seek help
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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 mutation in the DFNB59 gene on chromosome 2q31.
Resources
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