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Article

Phenotypic overlap of cardiac sodium channelopathies: individual-specific or mutation-specific?

Circulation journal : official journal of the Japanese Circulation Society - 1 May 2009

Makita Naomasa

Abstract excerpt

Mutations in the cardiac sodium channel gene SCN5A are responsible for a spectrum of hereditary arrhythmias, including type-3 long QT syndrome (LQT3), Brugada syndrome (BrS), conduction disturbance and sinus node dysfunction. These syndromes were originally regarded as independent entities with d...

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Identifiers

PMID: 19336922
DOI: 10.1253/circj.cj-09-0014

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19336922-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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