A novel mutation in the SCN5A gene is associated with Brugada syndrome-Reference-Cited by-同舟云学术

A novel mutation in the SCN5A gene is associated with Brugada syndrome

Published:2007-01 Issue:8 Volume:80 Page:716-724
ISSN:0024-3205
Container-title:Life Sciences
language:en
Short-container-title:Life Sciences

Author:

Shin Dong-Jik,Kim Eunmin,Park Sang-Bum,Jang Won-Cheoul,Bae Yoonsun,Han Jihye,Jang Yangsoo,Joung Boyoung,Lee Moon Hyoung,Kim Sung Soon,Huang Hai,Chahine Mohamed,Yoon Sungjoo Kim

Publisher

Elsevier BV

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference43 articles.

1. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome;Ackerman;The Journal of the American Medical Association,2001

2. A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome;Akai;FEBS Letters,2000

3. Electrical heterogeneity, cardiac arrhythmias, and sodium channel;Antzelevitch;Circulation Research,2001

4. Brugada syndrome: a decade of progress;Antzelevitch;Circulation Research,2002

5. Structure and function of the cardiac sodium channels;Balser;Cardiovascular Research,1999

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

2. Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome;HeartRhythm Case Reports;2021-02

3. Experimental Models of Brugada syndrome;International Journal of Molecular Sciences;2019-04-29

4. Patient-Specific and Genome-Edited Induced Pluripotent Stem Cell–Derived Cardiomyocytes Elucidate Single-Cell Phenotype of Brugada Syndrome;Journal of the American College of Cardiology;2016-11

5. Flecainide Provocation Reveals Concealed Brugada Syndrome in a Long QT Syndrome Family With a Novel L1786Q Mutation in SCN5A;Circulation Journal;2014