Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders-Reference-Cited by-同舟云学术

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

Published:2007-03-01 Issue:3 Volume:117 Page:765-772
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Mollet Julie,Giurgea Irina,Schlemmer Dimitri,Dallner Gustav,Chretien Dominique,Delahodde Agnès,Bacq Delphine,de Lonlay Pascale,Munnich Arnold,Rötig Agnès

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference29 articles.

1. Metabolism and function of coenzyme Q

2. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy.

3. Mitochondrial encephalomyopathy with coenzyme Q10 deficiency

4. A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency

5. Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency

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