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Association of GJB2 gene mutation with cochlear implant performance in genetic non-syndromic hearing loss

  • Published:2011-12 Issue:12 Volume:75 Page:1572-1575
  • ISSN:0165-5876
  • Container-title:International Journal of Pediatric Otorhinolaryngology
  • language:en
  • Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Karamert Recep,Bayazit Yildirim A.,Altinyay Senay,Yılmaz Akın,Menevse Adnan,Gokdogan Ozan,Gokdogan Cagil,Ant Ayca

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference23 articles.

1. Cracking the auditory genetic code: nonsyndromic hereditary hearing impairment;Lalwani;Am. J. Otol.,1999

2. Novel mutations in the Connexin 26 gene (GJB2) that cause 81 autosomal recessive (DFNB1) hearing loss;Kelley;Am. J. Hum. Genet.,1998

3. Connexin-26 mutations in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998

4. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins;Rabionet;Hum. Mutat.,2000

5. Connexin-associated deafness and speech perception outcome of cochlear implantation;Taitelbaum-Swead;Arch. Otolaryngol. Head Neck Surg.,2006

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