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2. Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes

6. Mitochondrial physiology: Gnaiger Erich et al ― MitoEAGLE Task Group

11. Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

17. COX10 Mutations Resulting in Complex Multisystem Mitochondrial Disease That Remains Stable Into Adulthood

20. Mitochondrial respiratory states and rates

35. Biochemical Diagnosis of Coenzyme Q10 Deficiency

37. Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

38. SURF1 deficiency: a multi-centre natural history study

41. Poor maternal nutrition followed by accelerated postnatal growth leads to alterations in DNA damage and repair, oxidative and nitrosative stress, and oxidative defense capacity in rat heart

42. Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions

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