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Article

SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias.

Journal of cardiovascular electrophysiology - 1 May 2006

Laitinen-Forsblom Päivi J, Mäkynen Pekka, Mäkynen Heikki, Yli-Mäyry Sinikka, Virtanen Vesa, Kontula Kimmo, Aalto-Setälä Katriina

Abstract excerpt

INTRODUCTION: We aimed at identifying the molecular defect underlying the clinical phenotype of a Finnish family with a cardiac conduction defect and atrial arrhythmias. METHODS AND RESULTS: A large Finnish family was clinically evaluated (ECG, 24-hour ambulatory ECG, echocardiography). We performed linkage analysis with markers flanking the SCN5A gene and subsequently sequenced the SCN5A gene. Five family...

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PMID: 16684018
DOI: 10.1111/j.1540-8167.2006.00411.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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