A novel ABCC2 p.G693R mutation resulting in loss of function of MRP2: a recurrent cause of hyperbilirubinemia in Dubin-Johnson syndrome in China
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J. Jia | X. Ou | H. You | A. Xu | Jian Huang | Yanmeng Li | Wei Zhang | Donghu Zhou | S. Jia | Yi Song | Lina Wu