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By Tiranti V.  

Human Molecular Genetics, Vol. 12, Iss. 4, 2003-02 ,pp. : 399-413

Oxford University Press

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A Single Cell Complementation Class is Common to Several Cases of Cytochrome c Oxidase-Defective Leigh's Syndrome

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Mimicking a SURF1 allele reveals uncoupling of cytochrome c oxidase assembly from translational regulation in yeast

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A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome

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Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2733-2742

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Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2

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Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 170-180

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