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See Latest ArticlesHomozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia
Pediatrics International, 07/28/09
Boo NY et al. – Homozygous variant of nucleotide 211 G-A mutation of UGT1A1 gene is a significant risk factor associated with severe hyperbilirubinemia among Malaysian Chinese newborns.
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