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Article

New familial heterozygous c 4066_4068 delTT 2 bp deletion of the SCN5A gene causing Brugada syndrome.

Heart rhythm - 1 Aug 2011

Möbius-Winkler Sven, Dähnert Ingo, Hindricks Gerhard, Schuler Gerhard, Adams Volker

Abstract excerpt

BACKGROUND: Cardiac sodium channel alterations have been identified as the underlying condition in patients with Brugada syndrome. OBJECTIVE: This study identified a novel mutation of the SCN5A gene in a family with Brugada syndrome. METHODS: Blood was drawn from the children and mother for genetic analysis. All exons of the SCN5A gene were amplified by polymerase chain reaction, and a sequence analysis was...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21397042
DOI: 10.1016/j.hrthm.2011.03.010

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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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