Research of genetic bases of hereditary non-syndromic hearing loss


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Subasioglu A. , Duman D., Sirmaci A., Bademci G., ÇARKIT F., SOMDAŞ M. A. , et al.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.52, ss.122-132, 2017 (ESCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 52 Konu: 3
  • Basım Tarihi: 2017
  • Doi Numarası: 10.5152/turkpediatriars.2017.4254
  • Dergi Adı: TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
  • Sayfa Sayısı: ss.122-132

Özet

Aim: Hearing loss is the most common sensory disorder that affects approximately one per 1000 live births. With this project, we aimed to identify gene variants that were common causes of hearing loss in Turkey to contribute to the planning of genetic screening programs for hearing loss, as well as to improve genetic counseling to affected families.