Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients

PURPOSE: Hearing loss is more prevalent in the Saudi Arabian population than in other populations; however, the full range of genetic etiologies in this population is unknown. We report the genetic findings from 33 Saudi hearing-loss probands of tribal ancestry, with predominantly prelingual severe...

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Sparad:
Bibliografiska uppgifter
I publikationen:Genet Med
Huvudupphovsmän: Almontashiri, Naif A M, Alswaid, Abdulrahman, Oza, Andrea, Al-Mazrou, Khalid A, Elrehim, Omnia, Tayoun, Ahmad Abou, Rehm, Heidi L, Amr, Sami S
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2018
Ämnen:
Original Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5929117/
https://ncbi.nlm.nih.gov/pubmed/29048421
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2017.143
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