Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus

Published:2008-11 Issue:11 Volume:10 Page:797-804
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Hildebrand Michael S.,Tack Dylan,McMordie Sarah J.,Deluca Adam,Hur In Ae,Nishimura Carla,Huygen Patrick,Casavant Thomas L.,Smith Richard J.H.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference28 articles.

1. van Camp G, Smith RJ. Hereditary Hearing Loss Homepage. Available at: http://webhost.ua.ac.be/hhh/. Accessed October 7, 2008.

2. Genes, hearing and deafness;Huygen,2007

Cited by 40 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. Cataloging Existing Hearing Loss Cohort Data to Guide the Development of Precision Medicine for Sensorineural Hearing Loss: A Systematic Review of Hearing Repositories;The Journal of International Advanced Otology;2023-10-02

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

3. The Pathological Mechanisms of Hearing Loss Caused by KCNQ1 and KCNQ4 Variants;Biomedicines;2022-09-12

4. AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss;Human Genetics;2022-01-17

5. Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss;Disease Models & Mechanisms;2021-11-01

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