Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report-Reference-Cited by-同舟云学术

Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report

Published:2020-07-24 Issue: Volume:7 Page:
ISSN:2297-055X
Container-title:Frontiers in Cardiovascular Medicine
language:
Short-container-title:Front. Cardiovasc. Med.

Author:

Nijak Aleksandra,Labro Alain J.,De Wilde Hans,Dewals Wendy,Peigneur Steve,Tytgat Jan,Snyders Dirk,Sieliwonczyk Ewa,Simons Eline,Van Craenenbroeck Emeline,Schepers Dorien,Van Laer Lut,Saenen Johan,Loeys Bart,Alaerts Maaike

Funder

Fonds Wetenschappelijk Onderzoek

European Research Council

Bijzonder Onderzoeksfonds

KU Leuven

Publisher

Frontiers Media SA

Subject

Cardiology and Cardiovascular Medicine

Reference27 articles.

1. About Brugada syndrome and its prevalence;Postema;Europace,2012

2. J wave syndromes: Brugada and early repolarization syndromes;Antzelevitch;Heart Rhythm,2015

3. Ion channels in the heart;Bartos;Compreh Physiol.,2015

4. Genetics of sudden cardiac death;Bezzina;Circ Res.,2015

5. Reduced penetrance and variable expression of SCN5A mutations and the importance of co-inherited genetic variants: case report and review of the literature;Robyns;Indian Pacing Electrophysiol J.,2014

Cited by 4 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. Biophysical mechanisms of myocardium sodium channelopathies;Pflügers Archiv - European Journal of Physiology;2024-03-01

2. Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts;Genes;2021-12-22

3. Functional Characterization of the Nemertide α Family of Peptide Toxins;Journal of Natural Products;2021-08-16

4. Clinical characterization of the first Belgian SCN5A founder mutation cohort;EP Europace;2020-11-22