(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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Identifiers
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