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Autosomal Recessive Nonsyndromic Deafness 123
An autosomal recessive nonsyndromic deafness characterized by bilateral severe to profound hearing impairment with onset as early as the first decade of life that is caused by homozygous mutation in the STX4 gene on chro
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Overview
An autosomal recessive nonsyndromic deafness characterized by bilateral severe to profound hearing impairment with onset as early as the first decade of life that is caused by homozygous mutation in the STX4 gene on chro
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