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Article

Mutational analysis of mitochondrial DNA in Brugada syndrome.

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology - 1 Jan 2000

Stocchi Laura, Polidori Emanuela, Potenza Lucia, Rocchi Marco Bruno Luigi, Calcabrini Cinzia, Busacca Paolo, Capalbo Maria, Potenza Domenico, Amati Francesca, Mango Ruggiero, Romeo Francesco, Novelli Giuseppe, Stocchi Vilberto

Abstract excerpt

BACKGROUND: Brugada syndrome (BrS) is a primary electrical disease associated with an increased risk of sudden cardiac death due to ventricular fibrillation. This pathology has nuclear heterogeneous genetic origins, and at present, molecular diagnostic tests on nuclear DNA cover only 30% of BrS patients. The aim of this study was to assess the possible involvement of mitochondrial (mt) DNA variants in BrS since...

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Identifiers

PMID: 26549652
DOI: 10.1016/j.carpath.2015.10.001

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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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