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Article

A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness

19 May 2009

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Share to Cardiac electrophysiology and arrhythmias
Share to Ion channel regulation and function
Share to Ion Channels and Receptors

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19648062
DOI: 10.1016/j.hrthm.2009.05.016

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Related research

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A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illnessPMID 19648062Read ↗

A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillationSemantic proximity Read ↗

[Clinical and electrocardiographic characteristics of carriers with SCN5A mutations and non-SCN5A mutations in fever-induced Brugada syndrome].Semantic proximity Read ↗

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Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What’s behind the scenes?Semantic proximity Read ↗

A single Na(+) channel mutation causing both long-QT and Brugada syndromes.Semantic proximity Read ↗

Genetic biomarkers in Brugada syndrome.Semantic proximity Read ↗

Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients.Semantic proximity Read ↗

Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutationSemantic proximity Read ↗

Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.Semantic proximity Read ↗

[SCN5A mutation in patients with Brugada electrocardiographic pattern induced by fever].Semantic proximity Read ↗

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