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Mitochondrial genome mutations in hypertensive individuals.

American journal of hypertension - 1 Jul 2004

Schwartz Faina, Duka Arvi, Sun Fengzhu, Cui Jing, Manolis Athanasios, Gavras Haralambos

Abstract excerpt

Human essential hypertension (HTN), a polygenic, multifactorial, and highly heterogeneous disorder of unknown etiology, has been shown to have excess maternal transmission in several studies, suggesting a possible mitochondrial involvement. In an effort to assess the contribution of the mitochondrial genome to HTN we initiated a systematic, extended screening of hypertensive individuals to identify potentially...

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PMID: 15233983
DOI: 10.1016/j.amjhyper.2004.02.020

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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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