Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA
Author:
Publisher
S. Karger AG
Subject
Speech and Hearing,Sensory Systems,Otorhinolaryngology,Physiology
Cited by 13 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. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01
2. Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss;Genes;2019-09-16
3. Characteristics of Mid-Frequency Sensorineural Hearing Loss Progression;Otology & Neurotology;2019-06
4. Hereditary hearing loss; about the known and the unknown;Hearing Research;2019-05
5. The European GWAS-identified risk SNP rs457717 within IQGAP2 is not associated with age-related hearing impairment in Han male Chinese population;European Archives of Oto-Rhino-Laryngology;2015-07-18
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