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  • Molecular assay reagents intended to identify deletions or duplications of the solute carrier family 25 member 4 (SLC25A4) gene, located at chromosome 4q35.1, which encodes the protein ADP/ATP translocase 1. Genetic variants at this locus have been associated with mitochondrial DNA depletion syndrome and progressive external ophthalmoplegia with mitochondrial DNA deletions.
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