Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)-Reference-Cited by-同舟云学术

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Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)

Published:2000-02 Issue:1 Volume:25 Page:45-54
ISSN:0307-7772
Container-title:Clinical Otolaryngology
language:en
Short-container-title:Clin Otolaryngol

Author:

Kunst H.,Marres H.,Huygen P.,Duijnhoven G.,Krebsova A.,Velde S.,Reis A.,Cremers F.,Cremers C.

Publisher

Wiley

Subject

Otorhinolaryngology

Reference24 articles.

1. Genetic Epidemiology of Hearing Impairment

2. Congenital hearing disability — epidemiology and identification: a comparison between two health authority districts

3. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

Cited by 30 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. RIPOR2: A new gene of non‐syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models;Clinical Genetics;2023-10-21

2. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01

3. A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss;Journal of Medical Genetics;2020-07-06

4. The Cation Channel TMEM63B Is an Osmosensor Required for Hearing;Cell Reports;2020-05

5. A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss;2019-12-23

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