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Autosomal Recessive Nonsyndromic Deafness 121
An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual moderate sensorineural hearing loss that is caused by homozygous or compound heterozygous mutation in the GPR156 gene on chromosome 3
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Overview
An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual moderate sensorineural hearing loss that is caused by homozygous or compound heterozygous mutation in the GPR156 gene on chromosome 3
Resources
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