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Autosomal Recessive Nonsyndromic Deafness 117
An autosomal recessive nonsyndromic deafness characterized by bilateral moderate-to-profound sensorineural deafness with onset in early childhood that is caused by homozygous mutation in the CLRN2 gene on chromosome 4p15
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Overview
An autosomal recessive nonsyndromic deafness characterized by bilateral moderate-to-profound sensorineural deafness with onset in early childhood that is caused by homozygous mutation in the CLRN2 gene on chromosome 4p15
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