Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients-Reference-Cited by-同舟云学术

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

Published:2018-05 Issue:5 Volume:20 Page:536-544
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Almontashiri Naif A.M.,Alswaid Abdulrahman,Oza Andrea,Al-Mazrou Khalid A.,Elrehim Omnia,Tayoun Ahmad Abou,Rehm Heidi L.,Amr Sami S.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2017143.pdf

Reference38 articles.

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Usher syndrome in the United Arab Emirates;Ophthalmic Genetics;2024-07-17

2. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22

3. Autoinhibition and activation of myosin VI revealed by its cryo-EM structure;Nature Communications;2024-02-08

4. The natural history, clinical outcomes, and genotype–phenotype relationship of otoferlin-related hearing loss: a systematic, quantitative literature review;Human Genetics;2023-09-07

5. Temperature-Sensitive Auditory Neuropathy: Report of a Novel Variant of OTOF Gene and Review of Current Literature;Medicina;2023-02-13

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