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[DOI] [PMC free article] [PubMed] [Google Scholar] 57.Burberry A, et al

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Homozygous mutations of the gene encoding Mrp2 (ABCC2) cause Dubin-Johnson syndrome, a rare liver disorder that presents with conjugated hyperbilirubinemia (Jemnitz et al., 2010)
doi: 10.1038/s41593-019-0532-y 294 SantosE

doi: 10.1002/glia.23645 31 DamierP.HirschE

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