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Autosomal Recessive Nonsyndromic Deafness 25
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and is caused by mutation in the GRXCR1 gene on chromosome 4p13.
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and is caused by mutation in the GRXCR1 gene on chromosome 4p13.
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