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Springer Publishing Company

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A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndrome

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Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 529-535

Oxford University Press

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Mitochondrial Complex I Deficiency in Humans

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Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons

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Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies

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Oxford University Press

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