Mutations in coenzyme Q10 biosynthetic genes
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference21 articles.
1. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy.
2. Mitochondrial encephalomyopathy with coenzyme Q10 deficiency
3. Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency
4. Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency
5. A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency
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