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Article

Mutational screening of SCN5A linked disorders in Polish patients and their family members.

Journal of applied genetics - 1 Jan 2004

Moric-Janiszewska Ewa, Herbert Ernest, Cholewa Krzysztof, Filipecki Artur, Trusz-Gluza Maria, Wilczok Tadeusz

Abstract excerpt

Mutations in SCN5A lead to a broad spectrum of phenotypes, including the Long QT syndrome, Brugada syndrome, Idiopathic ventricular fibrillation (IVF), Sudden infant death syndrome (SIDS) (probably regarded as a form of LQT3), Sudden unexplained nocturnal death syndrome (SUNDS) and isolated progressive cardiac conduction defect (PCCD) (Lev-Lenegre disease). Brugada Syndrome (BS) is a form of idiopathic...

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PMID: 15306732

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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