Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel

Prevention of Ventricular Fibrillation Episodes in Brugada Syndrome by Catheter Ablation Over the Anterior Right Ventricular Outflow Tract Epicardium

(2011) Koonlawee Nademanee et al.   CIRCULATION

MOG1

(2011) Darouna Kattygnarath et al.   Circulation-Cardiovascular Genetics

Transient outward current (Ito) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome

(2011) John R. Giudicessi et al.   HEART RHYTHM

Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

(2011) Birgit Stallmeyer et al.   HUMAN MUTATION

The transient receptor potential family of ion channels

(2011) Bernd Nilius et al.   GENOME BIOLOGY

Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction Disease

(2010) Hui Liu et al.   Circulation-Cardiovascular Genetics

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac KATP channel Kir6.1 as a pathogenic substrate for J-wave syndromes

(2010) Argelia Medeiros-Domingo et al.   HEART RHYTHM

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

(2010) Elena Burashnikov et al.   HEART RHYTHM

Right Ventricular Histological Substrate and Conduction Delay in Patients With Brugada Syndrome

(2010) Kimie Ohkubo et al.   International Heart Journal

Increased catecholamine secretion contributes to hypertension in TRPM4-deficient mice

(2010) Ilka Mathar et al.   JOURNAL OF CLINICAL INVESTIGATION

Physiological Roles of the TRPM4 Channel Extracted from Background Currents

(2010) Romain Guinamard et al.   PHYSIOLOGY

SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

(2009) Vincent Probst et al.   Circulation-Cardiovascular Genetics

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

(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

9-Phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels

(2008) T Grand et al.   BRITISH JOURNAL OF PHARMACOLOGY