Novel Mutations inSCO1as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis

COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux

(2013) Scot C. Leary et al.   MOLECULAR BIOLOGY OF THE CELL

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia

(2012) Radek Szklarczyk et al.   HUMAN MOLECULAR GENETICS

Unexpected Vascular Enrichment of SCO1 over SCO2 in Mammalian Tissues

(2010) Sonja Brosel et al.   AMERICAN JOURNAL OF PATHOLOGY

Loss of function of Sco1 and its interaction with cytochrome c oxidase

(2009) Lukas Stiburek et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

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

(2009) Scot C. Leary et al.   HUMAN MOLECULAR GENETICS

Suppression mechanisms of COX assembly defects in yeast and human: Insights into the COX assembly process

(2008) Antoni Barrientos et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH