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  • Molecular assay reagents intended to identify deletions or duplications of the COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor (COX10) gene, located at chromosome 17p12, which encodes the mitochondrial protein protoheme IX farnesyltransferase. Genetic variants at this locus have been associated with cytochrome-c oxidase deficiency and Leigh syndrome.
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