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Article

Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy.

Neuromuscular disorders : NMD - 1 Jan 2010

Sacconi Sabrina, Trevisson Eva, Salviati Leonardo, Aymé Ségolène, Rigal Odile, Redondo Alberto Garcia, Mancuso Michelangelo, Siciliano Gabriele, Tonin Paola, Angelini Corrado, Auré Karine, Lombès Anne, Desnuelle Claude

Abstract excerpt

Coenzyme Q(10) (CoQ(10)) deficiency has been associated with an increasing number of clinical phenotypes. Whereas primary CoQ(10) defects are related to mutations in ubiquinone biosynthetic genes, which are now being unraveled, and respond well to CoQ(10) supplementation, the etiologies, and clinical phenotypes related to secondary deficiencies are largely unknown. The purpose of this multicenter study was to...

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Identifiers

PMID: 19945282
DOI: 10.1016/j.nmd.2009.10.014

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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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