KCNE2 gene mutation and Brugada syndrome-Reference-Cited by-同舟云学术

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KCNE2 gene mutation and Brugada syndrome

Published:2021-03 Issue: Volume:65 Page:143-145
ISSN:0022-0736
Container-title:Journal of Electrocardiology
language:en
Short-container-title:Journal of Electrocardiology

Author:

Liatakis Ioannis,Pantou Malena P.,Gourzi Polyxeni,Bazoukis George,Mililis Panagiotis,Saplaouras Athanasios,Vlachos Konstantinos,Prappa Efstathia,Degiannis Dimitrios,Efremidis Michael,Letsas Konstantinos P.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference15 articles.

1. Present status of Brugada syndrome: JACC state-of-the-art review;Brugada;J Am Coll Cardiol,2018

2. Update on genetic basis of Brugada syndrome: monogenic, polygenic or Oligogenic?;Campuzano;Int J Mol Sci,2020

3. 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;Richards;Genet Med,2015

4. Genetic control of potassium channels;Amin;Card Electrophysiol Clin,2016

5. Effects of KCNE2 on HCN isoforms: distinct modulation of membrane expression and single channel properties;Brandt;Am J Physiol Heart Circ Physiol,2009

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pathophysiology of Atrial Fibrillation and Approach to Therapy in Subjects Less than 60 Years Old;International Journal of Molecular Sciences;2024-01-07

2. Genetics of sinoatrial node function and heart rate disorders;Disease Models & Mechanisms;2023-05-01

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