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Autosomal Recessive Nonsyndromic Deafness 119
An autosomal recessive nonsyndromic deafness characterized by mild to profound sensorineural hearing loss that is caused by compound heterozygous mutation in the AFG2B gene on chromosome 15q21.
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Overview
An autosomal recessive nonsyndromic deafness characterized by mild to profound sensorineural hearing loss that is caused by compound heterozygous mutation in the AFG2B gene on chromosome 15q21.
Resources
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