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A heteroplasmic, not homoplasmic, mitochondrial DNA mutation promotes tumorigenesis via alteration in reactive oxygen species generation and apoptosis
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A novel mitochondrial ND5 (MTND5) gene mutation giving. isolated exercise intolerance
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Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy
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An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria
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Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease
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Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF
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Minimum birth prevalence of mitochondrial respiratory chain disorders in children
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Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene
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Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria
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