SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
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Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death CasesThe Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritancePhysiological and Pathophysiological Insights of Nav1.4 and Nav1.5 ComparisonGenetics of inherited primary arrhythmia disordersCellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channelsElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesRecent advances in genetic testing and counseling for inherited arrhythmiasGenetics of Brugada syndromeCommon variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathGenetics of sudden cardiac death syndromesMolecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channelClinical and electrophysiological profile of Brugada syndrome in the Tunisian population.Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutationThe Diagnosis, Risk Stratification, and Treatment of Brugada SyndromeRisk Stratification and Therapeutic Approach in Brugada Syndrome.IRX3 variant as a modifier of Brugada syndrome with frequent ventricular fibrillationAn international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.A mutation in the CACNA1C gene leads to early repolarization syndrome with incomplete penetrance: A Chinese family study.Impact of genetics on the clinical management of channelopathies.SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility.J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledgeA novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndromeSCN5A variation is associated with electrocardiographic traits in the Jackson Heart Study.Complex genetic background in a large family with Brugada syndrome.Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathyFever-Induced Brugada Syndrome.Ionic and cellular mechanisms underlying the development of acquired Brugada syndrome in patients treated with antidepressants.SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathiesBrugada syndrome in a family with a high mortality rate: a case report.Cardiac sodium channel mutations: why so many phenotypes?Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification.Genetic Test for the Channelopaties: Useful or Less Than Useful for Patients? (Part II)Computational tools to investigate genetic cardiac channelopathies.Recent genetic discoveries implicating ion channels in human cardiovascular diseasesGenetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.Brugada syndrome: an update.Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects.Genetic testing for inherited cardiac disease.
P2860
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P2860
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@ast
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@en
type
label
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@ast
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@en
prefLabel
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@ast
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@en
P2093
P50
P1476
SCN5A mutations and the role o ...... hysiology of Brugada syndrome.
@en
P2093
Cedric Le Caignec
Dominique Babuty
Frederic Sacher
Hanno L Tan
Jacques Mansourati
Laetitia Gouas
Paola G Meregalli
Philippe Mabo
P304
P356
10.1161/CIRCGENETICS.109.853374
P50
P577
2009-09-29T00:00:00Z