Visualitzant Institut d’Investigació Biomèdica de Girona (IdIBGi) per matèria "Arrhythmia"

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

Genetics of channelopathies associated with sudden cardiac death

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances

Trafficking and Function of the Voltage-Gated Sodium Channel β2 Subunit

Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes