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  • Molecular assay reagents intended to identify mutations in the solute carrier family 25 (mitochondrial thiamine deoxynucleotide carrier), member 19 (SLC25A19) gene, located at chromosome 17q25.3, which encodes for a protein that transports thiamine pyrophosphate into the mitochondria. This inherited genetic mutation has been identified in patients with Amish lethal microcephaly.
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