Genes
SCO1
OMIMSynonym(s): SCOD1
Locus: 17p13.1
Protein: Protein SCO1 homolog
Disorder(s):
- Mitochondrial Respiratory Chain Complex IV Deficiency (Nuclear Genes)
- Hepatic Failure, Early-Onset, and Neurologic Disorder due to Cytochrome C Oxidase Deficiency
- Leigh Syndrome (nuclear DNA mutation)





