The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome-Reference-Cited by-同舟云学术

The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

Published:2008-05-01 Issue: Volume: Page:
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Makita Naomasa,Behr Elijah,Shimizu Wataru,Horie Minoru,Sunami Akihiko,Crotti Lia,Schulze-Bahr Eric,Fukuhara Shigetomo,Mochizuki Naoki,Makiyama Takeru,Itoh Hideki,Christiansen Michael,McKeown Pascal,Miyamoto Koji,Kamakura Shiro,Tsutsui Hiroyuki,Schwartz Peter J.,George Alfred L.,Roden Dan M.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference41 articles.

1. The Long QT Syndrome A Review of Recent Molecular Genetic and Physiologic Discoveries

2. Molecular mechanism for an inherited cardiac arrhythmia

3. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

4. Cardiac conduction defects associate with mutations in SCN5A

5. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

Cited by 41 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. Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants;Circulation: Genomic and Precision Medicine;2024-08

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

3. Development of automated patch clamp assays to overcome the burden of variants of uncertain significance in inheritable arrhythmia syndromes;Frontiers in Physiology;2023-11-27

4. ARumenamides: A novel class of potential antiarrhythmic compounds;Frontiers in Pharmacology;2022-09-28

5. Analysis of Augmentations for Contrastive ECG Representation Learning;2022 International Joint Conference on Neural Networks (IJCNN);2022-07-18