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  • Molecular assay reagents intended to identify mutations in the COX15 cytochrome c oxidase assembly homolog (COX15) gene, located at chromosome 10q24, which encodes the protein cytochrome c oxidase assembly protein COX15 homolog. Genetic variants at this locus have been associated with fetal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency 2 and Leigh syndrome.
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