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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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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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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OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules

By Yu-Wai-Man Patrick   Sitarz Kamil S.   Samuels David C.   Griffiths Philip G.   Reeve Amy K.   Bindoff Laurence A.   Horvath Rita   Chinnery Patrick F.  

Human Molecular Genetics, Vol. 19, Iss. 15, 2010-08 ,pp. : 3043-3052

Oxford University Press

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Mitochondrial complex I mutations in Caenorhabditis elegans produce cytochrome c oxidase deficiency, oxidative stress and vitamin-responsive lactic acidosis

By Grad Leslie I.   Lemire Bernard D.  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 303-314

Oxford University Press

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