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Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?

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

Khatami Mehri, Houshmand Massoud, Sadeghizadeh Majid, Eftekharzadeh Mahmood, Heidari Mohammad Mehdi, Saber Siamak, Banihashemi Kambiz, Scheiber-Mojdehkar Barbara

Abstract excerpt

BACKGROUND: Long QT syndrome (LQTS) is among arrhythmia disorders of the heart that causes sudden cardiac death in young individuals. As yet, most of investigations have focused on nuclear genome for finding genetic defects in this disorder, but some of the cases with LQTS cannot be explained by mutations of identified genes. On the other hand, it has been reported that the activity of ion channels in...

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PMID: 19369097
DOI: 10.1016/j.carpath.2008.12.009

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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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