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Article

[Clinical polymorphisms and approaches of arrhythmias treatment in a family with δKPQ1505-1507 deletion in SCN5A gene].

Vestnik Rossiiskoi akademii meditsinskikh nauk - 1 Jan 2014

Saber S, Houshmand M, Eftekhharzadeh M, Samiei Nasab, Fazelifar A F, Haghjoo M, Zakliaz'minskaia E V, Gavrilenko A V

Abstract excerpt

BACKGROUND: The aim of the study was to analyze spectrum of manifestation and treatment response in large family with rhythm disturbances caused by p.delKPQ1505-1507 mutation in SCN5A gene. PATIENTS AND METHODS: We had under our observation 18 members of large Iranian family with various combination of inherited arrhythmic syndromes. Careful cardiological examination, genetic councelling and venous blood sampling...

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PMID: 25558681
DOI: 10.15690/vramn.v69i5-6.1044

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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