Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference32 articles.
1. Newborn hearing screening—a silent revolution;CC Morton;N Engl J Med,2006
2. . Sensorineural hearing loss in children;RJ Smith;Lancet,2005
3. Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay;S Abe;Genet Test,2007
4. Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study;SI Usami;PLoS One,2012
5. Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing;AE Shearer;Proc Natl Acad Sci U S A,2010
Cited by 18 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. Identification of a novel mutation of EYA4 in a Chinese family with delayed nonsyndromic hearing loss and analysis of molecular epidemiology of EYA4 mutations;2024-03-25
2. Grainyhead-like 2 is required for morphological integrity of mouse embryonic stem cells and orderly formation of inner ear-like organoids;Frontiers in Cell and Developmental Biology;2023-09-07
3. Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants;Disease Models & Mechanisms;2023-08-01
4. The Pathological Mechanisms of Hearing Loss Caused by KCNQ1 and KCNQ4 Variants;Biomedicines;2022-09-12
5. Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss;Cells;2022-05-24
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