Clinical Heterogeneity in Sodium Channelopathies-Reference-Cited by-同舟云学术

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Clinical Heterogeneity in Sodium Channelopathies

Published:2007-10-31 Issue:2 Volume:110 Page:116-122
ISSN:0008-6312
Container-title:Cardiology
language:en
Short-container-title:Cardiology

Author:

Oliva Antonio,Bjerregaard Preben,Hong Kui,Evans Steven,Vernooy Kevin,McCormack Jorge,Brugada Josep,Brugada Pedro,Pascali Vincenzo L.,Brugada Ramon

Publisher

S. Karger AG

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine

Reference13 articles.

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

2. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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

4. Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

5. Genetics and Arrhythmias

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. SCN 2A channelopathies: Mechanisms and models;Epilepsia;2019-12

2. Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature;Indian Pacing and Electrophysiology Journal;2014-05

3. Diagnostic Electrocardiography;Electrical Diseases of the Heart;2013

4. Short QT Syndrome;Electrical Diseases of the Heart;2013

5. State of the Art in Forensic Investigation of Sudden Cardiac Death;American Journal of Forensic Medicine & Pathology;2011-03

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