Research of genetic bases of hereditary non-syndromic hearing loss

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...

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Bibliographic Details
Published in:Turk Pediatri Ars
Main Authors: Subaşıoğlu, Aslı, Duman, Duygu, Sırmacı, Aslı, Bademci, Güney, Carkıt, Fehime, Somdaş, Mehmet Akif, Erkan, Mustafa, Tekin, Mustafa, Dündar, Munis
Format: Artigo
Language:Inglês
Published: Turkish Pediatrics Association 2017
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Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5644578/
https://ncbi.nlm.nih.gov/pubmed/29062245
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2017.4254
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