Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese-Reference-Cited by-同舟云学术

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Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese

Published:2001-06 Issue:7 Volume:46 Page:355-361
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Akita J.,Abe S.,Shinkawa H.,Kimberling W. J.,Usami S.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg200166.pdf

Cited by 34 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. In vivo outer hair cell gene editing ameliorates progressive hearing loss in dominant-negative Kcnq4 murine model;Theranostics;2022

3. Progression of KCNQ4 related genetic hearing loss: a narrative review;Journal of Bio-X Research;2021-09-30

4. Molecular simulation of the Kv7.4[ΔS269] mutant channel reveals that ion conduction in the cavity is perturbed due to hydrophobic gating;Biochemistry and Biophysics Reports;2021-03

5. Clinical pathology and management of presbyacusis;Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics;2020-10-25

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