Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

Antzeko izenburuak

• Connexin26 deafness in several interconnected families
  nork: Wilcox, S., et al.
  Argitaratua: (1999)
• Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome
  nork: Hmani-Aifa, M, et al.
  Argitaratua: (2002)
• Sensorineural deafness inherited as a tissue specific mitochondrial disorder.
  nork: Jaber, L, et al.
  Argitaratua: (1992)
• Apparent phenotypic anticipation in autosomal dominant connexin 26 deafness
  nork: Sokolov, Meirav, et al.
  Argitaratua: (2014)
• Sensorineural deafness.
  nork: Douek, E
  Argitaratua: (1990)