SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome

10.1161/JAHA.116.005009

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Main Authors:	Makarawate, P, Chaosuwannakit, N, Vannaprasaht, S, Sahasthas, D, Koo, S.H, Lee, E.J.D, Tassaneeyakul, W, Barajas-Martinez, H, Hu, D, Sawanyawisuth, K
Other Authors:	DEPT OF PHARMACOLOGY
Format:	Article
Published:	2020
Subjects:	Article Brugada syndrome clinical article exon gene gene frequency gene mutation genetic polymorphism genetic variability genotype heart muscle conduction disturbance heart ventricle fibrillation heart ventricle tachycardia human implantable cardioverter defibrillator male PR interval priority journal QRS interval SCN5A gene single nucleotide polymorphism adult cardioversion devices electrocardiography female genetic association study genetic predisposition genetics heart muscle conduction system Kaplan Meier method middle aged pathophysiology phenotype Thailand time factor treatment outcome university hospital young adult SCN5A protein, human sodium channel Nav1.5 Adult Brugada Syndrome Defibrillators, Implantable Electric Countershock Electrocardiography Female Genetic Association Studies Genetic Predisposition to Disease Heart Conduction System Hospitals, University Humans Kaplan-Meier Estimate Male Middle Aged NAV1.5 Voltage-Gated Sodium Channel Phenotype Polymorphism, Genetic Time Factors Treatment Outcome Young Adult
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/178673
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1786732023-09-07T09:21:48Z SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome Makarawate, P Chaosuwannakit, N Vannaprasaht, S Sahasthas, D Koo, S.H Lee, E.J.D Tassaneeyakul, W Barajas-Martinez, H Hu, D Sawanyawisuth, K DEPT OF PHARMACOLOGY Article Brugada syndrome clinical article exon gene gene frequency gene mutation genetic polymorphism genetic variability genotype heart muscle conduction disturbance heart ventricle fibrillation heart ventricle tachycardia human implantable cardioverter defibrillator male PR interval priority journal QRS interval SCN5A gene single nucleotide polymorphism adult Brugada syndrome cardioversion devices electrocardiography female genetic association study genetic predisposition genetics heart muscle conduction system implantable cardioverter defibrillator Kaplan Meier method middle aged pathophysiology phenotype Thailand time factor treatment outcome university hospital young adult SCN5A protein, human sodium channel Nav1.5 Adult Brugada Syndrome Defibrillators, Implantable Electric Countershock Electrocardiography Female Genetic Association Studies Genetic Predisposition to Disease Heart Conduction System Hospitals, University Humans Kaplan-Meier Estimate Male Middle Aged NAV1.5 Voltage-Gated Sodium Channel Phenotype Polymorphism, Genetic Thailand Time Factors Treatment Outcome Young Adult 10.1161/JAHA.116.005009 Journal of the American Heart Association 6 6 e005009 2020-10-21T07:51:33Z 2020-10-21T07:51:33Z 2017 Article Makarawate, P, Chaosuwannakit, N, Vannaprasaht, S, Sahasthas, D, Koo, S.H, Lee, E.J.D, Tassaneeyakul, W, Barajas-Martinez, H, Hu, D, Sawanyawisuth, K (2017). SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome. Journal of the American Heart Association 6 (6) : e005009. ScholarBank@NUS Repository. https://doi.org/10.1161/JAHA.116.005009 20479980 https://scholarbank.nus.edu.sg/handle/10635/178673 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	Article Brugada syndrome clinical article exon gene gene frequency gene mutation genetic polymorphism genetic variability genotype heart muscle conduction disturbance heart ventricle fibrillation heart ventricle tachycardia human implantable cardioverter defibrillator male PR interval priority journal QRS interval SCN5A gene single nucleotide polymorphism adult Brugada syndrome cardioversion devices electrocardiography female genetic association study genetic predisposition genetics heart muscle conduction system implantable cardioverter defibrillator Kaplan Meier method middle aged pathophysiology phenotype Thailand time factor treatment outcome university hospital young adult SCN5A protein, human sodium channel Nav1.5 Adult Brugada Syndrome Defibrillators, Implantable Electric Countershock Electrocardiography Female Genetic Association Studies Genetic Predisposition to Disease Heart Conduction System Hospitals, University Humans Kaplan-Meier Estimate Male Middle Aged NAV1.5 Voltage-Gated Sodium Channel Phenotype Polymorphism, Genetic Thailand Time Factors Treatment Outcome Young Adult
spellingShingle	Article Brugada syndrome clinical article exon gene gene frequency gene mutation genetic polymorphism genetic variability genotype heart muscle conduction disturbance heart ventricle fibrillation heart ventricle tachycardia human implantable cardioverter defibrillator male PR interval priority journal QRS interval SCN5A gene single nucleotide polymorphism adult Brugada syndrome cardioversion devices electrocardiography female genetic association study genetic predisposition genetics heart muscle conduction system implantable cardioverter defibrillator Kaplan Meier method middle aged pathophysiology phenotype Thailand time factor treatment outcome university hospital young adult SCN5A protein, human sodium channel Nav1.5 Adult Brugada Syndrome Defibrillators, Implantable Electric Countershock Electrocardiography Female Genetic Association Studies Genetic Predisposition to Disease Heart Conduction System Hospitals, University Humans Kaplan-Meier Estimate Male Middle Aged NAV1.5 Voltage-Gated Sodium Channel Phenotype Polymorphism, Genetic Thailand Time Factors Treatment Outcome Young Adult Makarawate, P Chaosuwannakit, N Vannaprasaht, S Sahasthas, D Koo, S.H Lee, E.J.D Tassaneeyakul, W Barajas-Martinez, H Hu, D Sawanyawisuth, K SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome
description	10.1161/JAHA.116.005009
author2	DEPT OF PHARMACOLOGY
author_facet	DEPT OF PHARMACOLOGY Makarawate, P Chaosuwannakit, N Vannaprasaht, S Sahasthas, D Koo, S.H Lee, E.J.D Tassaneeyakul, W Barajas-Martinez, H Hu, D Sawanyawisuth, K
format	Article
author	Makarawate, P Chaosuwannakit, N Vannaprasaht, S Sahasthas, D Koo, S.H Lee, E.J.D Tassaneeyakul, W Barajas-Martinez, H Hu, D Sawanyawisuth, K
author_sort	Makarawate, P
title	SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome
title_short	SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome
title_full	SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome
title_fullStr	SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome
title_full_unstemmed	SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome
title_sort	scn5a genetic polymorphisms associated with increased defibrillator shocks in brugada syndrome
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/178673
_version_	1779152348202926080

SCN5A genetic polymorphisms associated with increased defibrillator shocks in Brugada syndrome

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