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A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis.

Neuromuscular disorders : NMD - 1 Feb 2004

McFarland Robert, Taylor Robert W, Chinnery Patrick F, Howell Neil, Turnbull Douglass M

Abstract excerpt

Disorders of the mitochondrial genome are an important cause of neurological disease, with patients presenting a variety of different phenotypes. Exercise induced muscle pain and myoglobinuria have been described with a number of metabolic defects, but because of the enormous variability of the mitochondrial genome identifying causative mitochondrial DNA mutations can be extremely difficult. Since mitochondrial...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 14733964
DOI: 10.1016/j.nmd.2003.10.011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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