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Autosomal Recessive Nonsyndromic Deafness 94
An autosomal recessive nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss that is caused by homozygous or compound heterozygous mutation in the NARS2 gene on chromosome 11q14.1.
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Overview
An autosomal recessive nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss that is caused by homozygous or compound heterozygous mutation in the NARS2 gene on chromosome 11q14.1.
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