Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes-Reference-Cited by-同舟云学术

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Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes

Published:2001-08 Issue:33 Volume:276 Page:30623-30630
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Rivolta Ilaria,Abriel Hugues,Tateyama Michihiro,Liu Huajun,Memmi Mirella,Vardas Panos,Napolitano Carlo,Priori Silvia G.,Kass Robert S.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference38 articles.

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

2. Cardiac conduction defects associate with mutations in SCN5A

3. A sodium-channel mutation causes isolated cardiac conduction disease

4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

5. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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