Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome SCN5A Mutation-Reference-Cited by-同舟云学术

Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome SCN5A Mutation

Published:2006-03 Issue:3 Volume:17 Page:270-275
ISSN:1045-3873
Container-title:Journal of Cardiovascular Electrophysiology
language:en
Short-container-title:J Cardiovasc Electrophysiol

Author:

PROBST VINCENT,ALLOUIS MARIE,SACHER FREDERIC,PATTIER SABINE,BABUTY DOMINIQUE,MABO PHILIPE,MANSOURATI JACQUES,VICTOR JACQUES,NGUYEN JEAN-MICHEL,SCHOTT JEAN-JACQUES,BOISSEAU PIERRE,ESCANDE DENIS,LE MAREC HERVE

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1540-8167.2006.00349.x/fullpdf

Reference18 articles.

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

2. Clinical and Genetic Heterogeneity of Right Bundle Branch Block and ST-Segment Elevation Syndrome

3. Cardiac conduction defects associate with mutations in SCN5A

4. Novel SCN5A Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family

5. Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

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