MOG1

Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model

(2010) Anne-Laure Leoni et al.   PLoS One

A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

(2009) Dan Hu et al.   Circulation-Cardiovascular Genetics

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test

(2009) Jamie D. Kapplinger et al.   HEART RHYTHM

The genetic basis of Brugada syndrome: A mutation update

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

Cardiac sodium channel Nav1.5 and interacting proteins: Physiology and pathophysiology

(2009) Hugues Abriel   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome

(2008) Eva Delpón et al.   Circulation-Arrhythmia and Electrophysiology

Identification of a New Co-factor, MOG1, Required for the Full Function of Cardiac Sodium Channel Nav1.5

(2008) Ling Wu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Voltage-gated Navchannel targeting in the heart requires an ankyrin-G–dependent cellular pathway

(2008) John S. Lowe et al.   JOURNAL OF CELL BIOLOGY

Cardiac Sodium Channel Overlap Syndromes: Different Faces of SCN5A Mutations

(2008) Carol Ann Remme et al.   TRENDS IN CARDIOVASCULAR MEDICINE