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  • Molecular assay reagents intended to identify mutations in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene, located at chromosome 1p36.3, which encodes for methylenetetrahydrofolate reductase enzyme involved in processing amino acids. Mutations at ths locus have been identified in patients with homocystinuria due to MTHFR deficiency and with premature atherosclerosis.
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