Associated Papers
Literature review and report of three cases of Dubin-Johnson syndrome related to ABCC2 gene mutations in children.
You SJ et al.
American Journal of Translational Research, 2021
A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China.
Wu L et al.
Orphanet Journal of Rare Diseases, 2020
32183854 (PubMed )
Supplement: 13023_2020_1346_MOESM1_ESM.docx
Identification of a compound heterozygous mutation of ABCC2 in a patient with hyperbilirubinemia.
Xiang R et al.
Molecular Medicine Reports, 2017
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