Polymorphism H558R in the Human Cardiac Sodium Channel SCN5A Gene is Associated with Atrial Fibrillation

A Brugada syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization

(2011) Stefano Marangoni et al.   CARDIOVASCULAR RESEARCH

Impact of Genetic Discoveries on the Classification of Lone Atrial Fibrillation

(2010) Jason D. Roberts et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Cardiac ion channels in health and disease

(2009) Ahmad S. Amin et al.   HEART RHYTHM

Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population

(2009) Lisong Shi et al.   HUMAN GENETICS

The genetic basis of Brugada syndrome: A mutation update

(2009) Paula L. Hedley et al.   HUMAN MUTATION

Genetic Modulation of Brugada Syndrome by a Common Polymorphism

(2009) ERIC LIZOTTE et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation

(2008) Dawood Darbar et al.   CIRCULATION

Epidemiology, Risk Factors for Stroke, and Management of Atrial Fibrillation in China

(2008) Dayi Hu et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Prolonged Signal-Averaged P-Wave Duration as an Intermediate Phenotype for Familial Atrial Fibrillation

(2008) Dawood Darbar et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation

(2008) Takeru Makiyama et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY