Sage Journals: Discover world-class research

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Research article

First published 2018-6

Dysfunctional Nav1.5 channels due to SCN5A mutations

Dan Han, Hui Tan, Chaofeng Sun [...]

Experimental Biology and Medicine

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Research article

First published 2015-06

An Investigation of the Association of the H558R Polymorphism of the SCN5A Gene with Idiopathic Cardiac Conduction Disorders

Svetlana Y. Nikulina, Anna A. Chernova, Vladimir A. Shulman [...]

Genetic Testing and Molecular Biomarkers

Free access

Research article

First published 2011-10

Polymorphism H558R in the Human Cardiac Sodium Channel SCN5A Gene is Associated with Atrial Fibrillation

L Chen, W Zhang, C Fang [...]

Journal of International Medical Research

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Research article

First published 2010-10

Alternative Promoter Usage and Splicing of the Human SCN5A Gene Contribute to Transcript Heterogeneity

Leonie van Stuijvenberg, Cansu Yildirim, Bart G.J.M. Kok [...]

DNA and Cell Biology

Open access

Research article

First published 2025

Genetic background and clinical phenotype in a Vietnamese cohort with Brugada syndrome: A whole exome sequencing study

Viet Tuan Tran, Hung Manh Pham, Phong Dinh Phan [...]

JRSM Cardiovascular Disease

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Brief report

First published 2003-03

Mutation Analysis in Congenital Long QT Syndrome—A Case with Missense Mutations in KCNQ1 and SCN5A

Aimée Paulussen, Gert Matthijs, Marc Gewillig [...]

Genetic Testing and Molecular Biomarkers

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Brief report

First published 2001-12

Genetic Analysis of Brugada Syndrome in Israel: Two Novel Mutations and Possible Genetic Heterogeneity

Etgar Levy-Nissenbaum, Michael Eldar, Qing Wang [...]

Genetic Testing and Molecular Biomarkers

Open access

Case report

First published 2024

Type I Brugada Pattern in a Febrile Patient Following COVID-19 Vaccination Booster

Robert Cacdac, Anthony Lim, Jonathan Ghazaleh [...]

Journal of Investigative Medicine High Impact Case Reports

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Research article

First published 2005-12

Gene Sequencing in Neonates and Infants with the Long QT Syndrome

Sung Han Shim, Masamichi Ito, Thomas Maher [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2024-05

The Beneficial Role of Telemedicine for Arrhythmic Risk Stratification in Asymptomatic Brugada Syndrome: An Exemplary Case Report

Vincenzo Ezio Santobuono, Maria Cristina Carella, Andrea Igoren Guaricci [...]

Telemedicine and e-Health

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