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Autosomal Recessive Nonsyndromic Deafness 114
An autosomal recessive nonsyndromic deafness characterized by congenital profound sensorineural hearing loss that is caused by homozygous or compound heterozygous mutation in the GRAP gene on chromosome 17p11.2.
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Overview
An autosomal recessive nonsyndromic deafness characterized by congenital profound sensorineural hearing loss that is caused by homozygous or compound heterozygous mutation in the GRAP gene on chromosome 17p11.2.
Resources
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