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Dear Editor,We read with great interest the letter by D’Apolito et al, Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia .[1][1] The authors analysed UGT1A1 gene in 11 unrelated patients with neonatal hyperbilirubinemia. They described seven novel

Comments on Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia by D'Apolito et al.