| 1 | ABCC2, DJS
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| Neonatal Dubin-Johnson syndrome: long-term follow-up and MRP2 mutations study.
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| Lee JH, Chen HL, Chen HL, Ni YH, Hsu HY, Chang MH.
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| Pediatr Res 59(4 Pt 1):584-9. 2006
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| 2 | ABCC2, DJS
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| Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in dubin-johnson syndrome.
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| Toh S, et al.
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| Am J Hum Genet 64(3):739-46. 1999
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| 3 | ABCC2, DJS
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| Mutations in the canalicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome.
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| Wada M, Toh S, Taniguchi K, Nakamura T, Uchiumi T, Kohno K, Yoshida I, Kimura A, Sakisaka S, Adachi Y, Kuwano M.
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| Hum Mol Genet 7(2):203-7. 1998
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| 4 | ABCC2, DJS
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| A splice mutation in the human canalicular multispecific organic anion transporter gene causes Dubin-Johnson syndrome.
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| Kajihara S, et al.
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| Biochem Biophys Res Commun 253(2):454-7. 1998
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| 5 | ABCC2, DJS
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| A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome.
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| Paulusma CC, Kool M, Bosma PJ, Scheffer GL, ter Borg F, Scheper RJ, Tytgat GN, Borst P, Baas F, Oude Elferink RP.
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| Hepatology 25(6):1539-42. 1997
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| 6 | ABCC2, DJS
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| Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19D2 by fluorescent in situ hybridization.
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| van Kuijck MA, Kool M, Merkx GF, Geurts van Kessel A, Bindels RJ, Deen PM, van Os CH.
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| Cytogenet Cell Genet 77(3-4):285-7. 1997
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