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Autosomal Recessive Nonsyndromic Deafness 57
An autosomal recessive nonsyndromic deafness characterized by symmetric bilateral moderate to severe hearing loss that is caused by homozygous or compound heterozygous mutation in the PDZD7 gene on chromosome 10q24.31.
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Overview
An autosomal recessive nonsyndromic deafness characterized by symmetric bilateral moderate to severe hearing loss that is caused by homozygous or compound heterozygous mutation in the PDZD7 gene on chromosome 10q24.31.
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