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  • Molecular assay reagents intended to identify mutations in the UDP glycosyltransferase 1 family, polypeptide A1 (UGT1A1) gene, located at chromosome 2q37, which encodes for an enzyme that is important in the conjugation and elimination of toxic xenobiotics and endogenous compounds. This inherited genetic mutation has been identified in patients with Crigler-Najjar syndrome types I and II.
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