Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family-Reference-Cited by-同舟云学术

Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family

Published:2010-07 Issue:2 Volume:142 Page:206-208
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Zamorano-León José J.,Alonso-Orgaz Sergio,Moreno Javier,Cinza Rafael,García-Torrent Maria J.,Pérez-Castellano Nicasio,Pérez-Villacastín Julián,Macaya Carlos,López-Farré Antonio J.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference7 articles.

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2. Genomics and cardiac arrhythmias;Roberts;J Am Coll Cardiol,2006

3. Low penetrance in the long-QT syndrome: clinical impact;Priori;Circulation,1999

4. Arrhytmogenic right ventricular cardiomiopathy with palmoplantar keratoderma in a Spanish patient without plakoglobin and desmoplakin gene modifications;Alonso-Orgaz;Int J Cardiol,2007

5. Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes;Zhang;Circulation,2000

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1. Stress status and ventricular fibrillation in long QT syndrome;International Journal of Cardiology;2014-04

2. Platelet Content of Nitric Oxide Synthase 3 Phosphorylated At Serine1177 Is Associated with the Functional Response of Platelets to Aspirin;PLoS ONE;2013-12-20

3. KCNH2 Gene Mutation: A Potential Link Between Epilepsy and Long QT-2 Syndrome;Journal of Neurogenetics;2012-04-19