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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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| Wydane w: | Turk Pediatri Ars |
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| Główni autorzy: | , , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Turkish Pediatrics Association
2017
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| Hasła przedmiotowe: | |
| Dostęp online: | 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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