(Q28024653)
English
autosomal recessive nonsyndromic deafness 79
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the TPRN gene on chromosome 9q34
- DFNB79
- autosomal recessive deafness 79
- DEAFNESS, AUTOSOMAL RECESSIVE 79; DFNB79
- autosomal recessive nonsyndromic deafness type 79
- DEAFNESS, AUTOSOMAL RECESSIVE 79
- Deafness, Autosomal Recessive type 79
Statements
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Identifiers
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