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Autosomal Recessive Nonsyndromic Deafness 112
An autosomal recessive nonsyndromic deafness characterized by postlingual progressive sensorineural hearing impairment that is caused by homozygous or compound heterozygous mutation in the BDP1 gene on chromosome 5q13.2.
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Overview
An autosomal recessive nonsyndromic deafness characterized by postlingual progressive sensorineural hearing impairment that is caused by homozygous or compound heterozygous mutation in the BDP1 gene on chromosome 5q13.2.
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