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Article

Update of diagnosis and management of inherited cardiac arrhythmias.

Circulation journal : official journal of the Japanese Circulation Society - 1 Jan 2013

Shimizu Wataru

Abstract excerpt

Over the past 2 decades, a number of inherited cardiac arrhythmias, including congenital long QT syndrome (LQTS) and Brugada syndrome (BrS), have been shown to have a link to mutations in genes encoding for ion channels or other membrane components. The recent HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited arrhythmia syndromes has updated the clinical...

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Share to Brugada Syndrome
Share to Cardiac Arrhythmias and Treatments
Share to Cardiac electrophysiology and arrhythmias

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Ion channel regulation and function

Share to Long QT Syndrome

Share to Mutation

Share to Polymorphism, Genetic

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Identifiers

PMID: 24200848
DOI: 10.1253/circj.cj-13-1217

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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