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- [21] Identification of a novel 974C→G nonsense mutation of the MRP2/ABCC2 gene in a patient with Dubin-Johnson syndrome and analysis of the effects of rifampicin and ursodeoxycholic acid on serum bilirubin and bile acids AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (10): : 2427 - 2432
- [23] A novel homozygous frameshift variant in the ABCC2-gene in Dubin-Johnson syndrome may predispose to chronic liver disease Indian Journal of Gastroenterology, 2021, 40 : 72 - 76
- [27] A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China Orphanet Journal of Rare Diseases, 15
- [30] Homozygous mutation Arg768Trp in the ABC-transporter encoding gene MRP2/cMOAT/ABCC2 causes Dubin-Johnson syndrome in a Caucasian patient Journal of Human Genetics, 2003, 48 : 484 - 486