Dubin-johnson Syndrome
What's New
Last Posted: Mar 04, 2023
- Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.
Corpechot Christophe, et al. Liver international : official journal of the International Association for the Study of the Liver 2019 0 (1) 163-174 - [Genetic analysis of a case with Dubin-Johnson syndrome due to two novel variants of ABCC2 gene].
Zhao Ganye, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 0 (9) 974-978 - Dubin-Johnson syndrome in Tunisia: Spectrum of a rare disease.
Guirat Naouel et al. Presse medicale (Paris, France : 1983) 2019 Jan 48(1 Pt 1) 81-82 - Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing.
Togawa Takao, et al. The Journal of pediatrics 2016 2 - Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.
Slachtova Lenka, et al. European journal of human genetics : EJHG 2015 9 - Urinary elimination of coproporphyrins is dependent on ABCC2 polymorphisms and represents a potential biomarker of MRP2 activity in humans.
Benz-de Bretagne I, et al. Journal of biomedicine & biotechnology 2011 5 - Dubin-Johnson syndrome
From NCATS Genetic and Rare Diseases Information Center
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- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
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