A Novel mutation L619F in the cardiac Na channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A Novel mutation L619F in the cardiac Na channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating

Published:2003-05 Issue:5 Volume:21 Page:552-552
ISSN:1059-7794
Container-title:Human Mutation
language:
Short-container-title:Hum. Mutat.

Author:

Wehrens Xander H.T.,Rossenbacker Tom,Jongbloed Roselie J.,Gewillig Marc,Heidbüchel Hein,Doevendans Pieter A.,Vos Marc A.,Wellens Hein J.J.,Kass Robert S.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 33 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. Biophysical mechanisms of myocardium sodium channelopathies;Pflügers Archiv - European Journal of Physiology;2024-03-01

2. In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome;Molecular Genetics & Genomic Medicine;2023-08-07

3. Cardiolipotoxicity, Inflammation, and Arrhythmias: Role for Interleukin-6 Molecular Mechanisms;Frontiers in Physiology;2019-01-07

4. An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation;Scientific Reports;2018-10-02

5. Arrhythmias precede cardiomyopathy and remodeling of Ca2+ handling proteins in a novel model of long QT syndrome;Journal of Molecular and Cellular Cardiology;2018-10

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