Genotype–phenotype relationship and risk stratification in loss‐of‐function SCN 5A mutation carriers-Reference-Cited by-同舟云学术

Genotype–phenotype relationship and risk stratification in loss‐of‐function SCN 5A mutation carriers

Published:2018-04-30 Issue:5 Volume:23 Page:
ISSN:1082-720X
Container-title:Annals of Noninvasive Electrocardiology
language:en
Short-container-title:Ann Noninvasive Electrocardiol

Author:

Robyns Tomas¹²^ORCID,Nuyens Dieter³,Vandenberk Bert¹²,Kuiperi Cuno⁴,Corveleyn Anniek⁴,Breckpot Jeroen⁴,Garweg Christophe¹²,Ector Joris¹²,Willems Rik¹²

Affiliation:

1. Department of Cardiovascular DiseasesUniversity Hospitals Leuven Leuven Belgium

2. Department of Cardiovascular SciencesUniversity of Leuven Leuven Belgium

3. Department of CardiologyZiekenhuis Oost Limburg Genk Belgium

4. Department of Human GeneticsUniversity Hospitals Leuven Leuven Belgium

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/anec.12548

Reference38 articles.

1. Comparison of Late Potentials for 24 Hours Between Brugada Syndrome and Arrhythmogenic Right Ventricular Cardiomyopathy Using a Novel Signal-Averaging System Based on Holter ECG

2. Assessment of Markers for Identifying Patients at Risk for Life-Threatening Arrhythmic Events in Brugada Syndrome

3. J‐Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge: Endorsed by the Asia Pacific Heart Rhythm Society (APHRS), the European Heart Rhythm Association (EHRA), the Heart Rhythm Society (HRS), and the Latin American Society of Cardiac Pacing and Electrophysiology (Sociedad Latinoamericana de Estimulacifin Cardíaca y Electrofisiología [SOLAECE]);Antzelevitch C.;Europace,2017

4. Long-Term Follow-Up of Probands With Brugada Syndrome

5. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

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1. SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis;Heart Rhythm;2024-04

2. A novel association between sinus node dysfunction and an SCN5A variant presenting as persistent symptomatic bradycardia in a young adult;HeartRhythm Case Reports;2023-09

3. The SCN5A gene is a phenotype severity predictor in Brugada syndrome – a comprehensive literature review;Medical Principles and Practice;2022-11-29

4. Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands;Circulation: Genomic and Precision Medicine;2021-10

5. Identification of Novel SCN5A Single Nucleotide Variants in Brugada Syndrome: A Territory-Wide Study From Hong Kong;Frontiers in Physiology;2020-09-18