A novelSCN5Amutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome-Reference-Cited by-同舟云学术

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A novelSCN5Amutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome

Published:2000-08-07 Issue:1-2 Volume:479 Page:29-34
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Akai Jun,Makita Naomasa,Sakurada Harumizu,Shirai Nobumasa,Ueda Kazuo,Kitabatake Akira,Nakazawa Kiyoshi,Kimura Akinori,Hiraoka Masayasu

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(00)01875-5/fullpdf

Reference20 articles.

1. Idiopathic Ventricular Tachycardia and Fibrillation

2. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

3. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

4. A Single Na + Channel Mutation Causing Both Long-QT and Brugada Syndromes

5. Genomic Organization of the HumanSCN5AGene Encoding the Cardiac Sodium Channel

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