KCNE2 gene mutation and Brugada syndrome.

[1]  J. Brugada,et al.  Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic? , 2020, International journal of molecular sciences.

[2]  J. Brugada,et al.  Present Status of Brugada Syndrome: JACC State-of-the-Art Review. , 2018, Journal of the American College of Cardiology.

[3]  J. Healey,et al.  Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? , 2017, Circulation. Arrhythmia and electrophysiology.

[4]  A. Wilde,et al.  Genetic Control of Potassium Channels. , 2016, Cardiac electrophysiology clinics.

[5]  Alessandro Pietrelli,et al.  High-throughput genetic characterization of a cohort of Brugada syndrome patients. , 2015, Human molecular genetics.

[6]  Bale,et al.  Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology , 2015, Genetics in Medicine.

[7]  G. Wang,et al.  KCNE2 modulates cardiac L-type Ca(2+) channel. , 2014, Journal of molecular and cellular cardiology.

[8]  Yingying Tang,et al.  Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths. , 2014, Forensic science international.

[9]  D. Tester,et al.  Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing. , 2012, Mayo Clinic proceedings.

[10]  J. Towbin,et al.  KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders. , 2010, Heart rhythm.

[11]  U. Hoppe,et al.  Effects of KCNE2 on HCN isoforms: distinct modulation of membrane expression and single channel properties. , 2009, American journal of physiology. Heart and circulatory physiology.

[12]  J. M. Di Diego,et al.  A transient outward potassium current activator recapitulates the electrocardiographic manifestations of Brugada syndrome. , 2008, Cardiovascular research.

[13]  S. Bendahhou,et al.  Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. , 2004, American journal of human genetics.

[14]  D M Roden,et al.  A common polymorphism associated with antibiotic-induced cardiac arrhythmia. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[15]  M. Keating,et al.  MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia , 1999, Cell.