(Q28024600)

English

autosomal recessive nonsyndromic deafness 1A

autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has material basis in mutation in the GJB2 gene on chromosome 13q12

  • DFNB1A
  • autosomal recessive deafness 1A
  • autosomal recessive nonsyndromic hearing loss 1A

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