Cytochrome c oxidase deficiency due to mutations in SCO2 , encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

By Jaksch Michaela  

Human Molecular Genetics, Vol. 10, Iss. 26, 2001-12 ,pp. : 3025-3035

Oxford University Press

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

By Yang Hua   Brosel Sonja   Acin-Perez Rebeca   Slavkovich Vesna   Nishino Ichizo   Khan Raffay   Goldberg Ira J.   Graziano Joseph   Manfredi Giovanni   Schon Eric A.  

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

Oxford University Press

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Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

By Jaksch Michaela  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 795-801

Oxford University Press

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Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1

By Leary Scot C.   Sasarman Florin   Nishimura Tamiko   Shoubridge Eric A.  

Human Molecular Genetics, Vol. 18, Iss. 12, 2009-06 ,pp. : 2230-2240

Oxford University Press

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Transcriptional activators HAP/NF-Y rescue a cytochrome c oxidase defect in yeast and human cells

By Fontanesi Flavia   Jin Can   Tzagoloff Alexander   Barrientos Antoni  

Human Molecular Genetics, Vol. 17, Iss. 6, 2008-03 ,pp. : 775-788

Oxford University Press

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