Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase

By Leary Scot C.  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1839-1848

Oxford University Press

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

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

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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

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

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

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An isoform of Pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes

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Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1195-1205

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