The human Nav1.5 F1486 deletion associated with long QT syndrome leads to impaired sodium channel inactivation and reduced lidocaine sensitivity

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel

(2011) Arthur A.M. Wilde et al.   CIRCULATION RESEARCH

Trafficking Defects and Gating Abnormalities of a Novel SCN5A Mutation Question Gene-Specific Therapy in Long QT Syndrome Type 3

(2010) Yanfei Ruan et al.   CIRCULATION RESEARCH

Human voltage-gated sodium channel mutations that cause inherited neuronal and muscle channelopathies increase resurgent sodium currents

(2010) Brian W. Jarecki et al.   JOURNAL OF CLINICAL INVESTIGATION

Sodium Channel Molecular Conformations and Antiarrhythmic Drug Affinity

(2010) Michael F. Sheets et al.   TRENDS IN CARDIOVASCULAR MEDICINE

Phenotypic Overlap of Cardiac Sodium Channelopathies

(2009) Naomasa Makita   CIRCULATION JOURNAL

Using Lidocaine and Benzocaine to Link Sodium Channel Molecular Conformations to State-Dependent Antiarrhythmic Drug Affinity

(2009) Dorothy A. Hanck et al.   CIRCULATION RESEARCH

The genetic basis of long QT and short QT syndromes: A mutation update

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

A novel SCN5A mutation associated with the linker between III and IV domains of Nav1.5 in a neonate with fatal long QT syndrome

(2009) Kenichiro Yamamura et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Cardiac sodium channelopathies

(2009) Ahmad S. Amin et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

An increase of late sodium current induces delayed afterdepolarizations and sustained triggered activity in atrial myocytes

(2008) Yejia Song et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

SCN5A overlap syndromes: no end to disease complexity?

(2008) C. A. Remme et al.   EUROPACE

Paroxysmal extreme pain disorder mutations within the D3/S4-S5 linker of Nav1.7 cause moderate destabilization of fast inactivation

(2008) Brian W. Jarecki et al.   JOURNAL OF PHYSIOLOGY-LONDON

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

Cardiac Sodium Channel Overlap Syndromes: Different Faces of SCN5A Mutations

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