Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy-Reference-Cited by-同舟云学术

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

Published:2010-01 Issue:1 Volume:20 Page:44-48
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

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

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference32 articles.

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2. Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes;Montero;Clin Biochem,2008

3. Functional characterization of human COQ4, a gene required for coenzyme Q10 biosynthesis;Casarin;Biochem Biophys Res Commun,2008

4. Specificity of coenzyme Q10 for a balanced function of respiratory chain and endogenous ubiquinone biosynthesis in human cells;Fernandez-Ayala;Biochim Biophys Acta,2005

5. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy;Ogasahara;Proc Natl Acad Sci USA,1989

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