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Pending robust clinical evidence generation, a prudent individualized approach incorporating appropriate monitoring remains warranted

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Eur J Med Genet 1(71):104962 Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K et al (2016) Genotype of UGT1A1 and phenotype correlation between CriglerNajjar syndrome type II and Gilbert syndrome