Clinical Profiles of DFNA11 at Diverse Stages of Development and Aging in a Large Family Identified by Linkage Analysis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Clinical Profiles of DFNA11 at Diverse Stages of Development and Aging in a Large Family Identified by Linkage Analysis

Published:2020-02-25 Issue:6 Volume:41 Page:e663-e673
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Yamamoto Nobuko,Mutai Hideki,Namba Kazunori,Goto Fumiyuki,Ogawa Kaoru,Matsunaga Tatsuo

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference47 articles.

1. Sensorineural hearing loss in children;Smith;Lancet,2005

2. Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia;Weil;Proc Natl Acad Sci USA,1996

3. Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction;Grati;Proc Natl Acad Sci USA,2011

4. UniProt: the universal protein knowledgebase;Nucleic Acids Res,2018

5. The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies;Stenson;Hum Genet,2017

Cited by 5 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 caused by a novel mutation in MYO7A: A case report and review of the literature;World Journal of Clinical Cases;2023-09-06

2. Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains;Biomedicines;2022-03-29

3. Diagnostic Yield of Targeted Hearing Loss Gene Panel Sequencing in a Large German Cohort With a Balanced Age Distribution from a Single Diagnostic Center;Ear & Hearing;2021-11-08

4. Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease;Hearing Research;2021-09

5. Functional Role of Class III Myosins in Hair Cells;Frontiers in Cell and Developmental Biology;2021-02-25

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3