Characterization and Mechanisms of Action of Novel Na V 1.5 Channel Mutations Associated With Brugada Syndrome-Reference-Cited by-同舟云学术

Characterization and Mechanisms of Action of Novel Na V 1.5 Channel Mutations Associated With Brugada Syndrome

Published:2013-02 Issue:1 Volume:6 Page:177-184
ISSN:1941-3149
Container-title:Circulation: Arrhythmia and Electrophysiology
language:en
Short-container-title:Circ Arrhythm Electrophysiol

Author:

Calloe Kirstine¹,Refaat Marwan M.¹,Grubb Soren¹,Wojciak Julianne¹,Campagna Joan¹,Thomsen Nancy Mutsaers¹,Nussbaum Robert L.¹,Scheinman Melvin M.¹,Schmitt Nicole¹

Affiliation:

1. From the Danish National Research Foundation Centre for Cardiac Arrhythmia and Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark (K.C., S.G., N.M.T., N.S.); and Department of Medicine, University of California San Francisco, San Francisco, CA (M.M.R., J.W., J.C., R.L.N., M.M.S.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference20 articles.

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

2. Is the Brugada Syndrome a Distinct Clinical Entity?

3. Brugada Syndrome: Report of the Second Consensus Conference

4. Gender Differences in Clinical Manifestations of Brugada Syndrome

5. The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome

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