Publication | Open Access

Mutations of the SCO1 Gene in Mitochondrial Cytochrome c Oxidase Deficiency with Neonatal-Onset Hepatic Failure and Encephalopathy

HepatologyMitochondrial FunctionBiochemistryLiver PhysiologyGeneticsNeonatal-onset Hepatic FailurePathologySco1 GeneHepatotoxicityReactive Oxygen SpecieMetabolismMedicineRedox BiologyOxidative Stress