The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population

Asli Sirmaci, Duygu Akcayoz-Duman, Mustafa Tekin

Research output: Contribution to journalArticlepeer-review

41 Scopus citations
Original languageEnglish (US)
Pages (from-to)213-216
Number of pages4
JournalJournal of Genetics
Issue number3
StatePublished - Dec 2006
Externally publishedYes


  • Connexin26
  • Connexin30
  • Deafness
  • Gap junctions
  • GJB2
  • GJB6
  • Hearing impairment

ASJC Scopus subject areas

  • Genetics

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