GJB2 mutations in Turkish patients with nonsyndromic hearing loss

EYERCİ N., ALTAŞ E., Pirim I.

META GENE, cilt.10, ss.56-60, 2016 (ESCI, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 10
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.mgene.2016.10.006
  • Dergi Adı: META GENE
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus
  • Sayfa Sayıları: ss.56-60
  • Atatürk Üniversitesi Adresli: Evet

Özet

Aim: Mutations in the GJB2 gene are the most common cause of non-syndromic recessive hearing loss all around the world. We aim to describe the genotype distributions and auditory phenotype of Turkish patients with congenital hearing loss in the east of Turkey.