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Autosomal Recessive Nonsyndromic Deafness 61
An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and is caused by mutation in the SLC26A5 gene on chromosome 7q22.
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and is caused by mutation in the SLC26A5 gene on chromosome 7q22.
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