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  • Andras Bors, Hajnalka Andrikovics, +7 authors Attila Tordai
  • Biology, Medicine
  • International journal of molecular medicine
  • 2004 (First Publication: 1 December 2004)
  • The most common form of non-syndromic autosomal recessive deafness (NSRD) is caused by mutations in the gene GJB2, encoding the protein connexin 26 (Cx26). The mutation c.35delG is found in 30-70% ofExpand