(Q28024646)

English

autosomal recessive nonsyndromic deafness 68

autosomal recessive nonsyndromic deafness that has material basis in mutation in the S1PR2 gene on chromosome 19p13

  • DFNB68
  • autosomal recessive deafness 68
  • autosomal recessive nonsyndromic deafness type 68
  • DEAFNESS, AUTOSOMAL RECESSIVE 68; DFNB68
  • DEAFNESS, AUTOSOMAL RECESSIVE 68

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