Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss-Reference-Cited by-同舟云学术

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Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss

Published:2003-04-01 Issue:4 Volume:129 Page:411
ISSN:0886-4470
Container-title:Archives of Otolaryngology–Head & Neck Surgery
language:en
Short-container-title:Arch Otolaryngol Head Neck Surg

Author:

Lesperance Marci M.,Hall James W.,San Agustin Theresa B.,Leal Suzanne M.

Publisher

American Medical Association (AMA)

Subject

General Medicine,Otorhinolaryngology,Surgery

Cited by 55 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. Wfs1E864K knock-in mice illuminate the fundamental role of Wfs1 in endocochlear potential production;Cell Death & Disease;2023-06-29

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

3. Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38;Genes;2023-02-10

4. Wfs1E864K knock-in mice illuminate the fundamental role of Wfs1 in endocochlear potential production;2023-01-31

5. Monogenic Causes of Low-Frequency Non-Syndromic Hearing Loss;Audiology and Neurotology;2023

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