Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver

Author:

van de Steeg Evita,Stránecký Viktor,Hartmannová Hana,Nosková Lenka,Hřebíček Martin,Wagenaar Els,van Esch Anita,de Waart Dirk R.,Oude Elferink Ronald P.J.,Kenworthy Kathryn E.,Sticová Eva,al-Edreesi Mohammad,Knisely A.S.,Kmoch Stanislav,Jirsa Milan,Schinkel Alfred H.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference54 articles.

1. Chowdhury JR, Chowdhury NR, Jansen PLM. Bilirubin metabolism and its disorders. In: Boyer TD, Wright TL, Manns MP, Zakim D, eds.Zakim and Boyer’s Hepatology. A Textbook of Liver Diseases . Vol. 2. Philadelphia, Pennsylvania, USA: Saunders Elsevier; 2006:1449–1474.

2. Chowdhury JR, Wolkoff AW, Chowdhury NR, Arias IM. Hereditary jaundice and disorders of bilirubin metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic and Molecular Bases of Inherited Disease . Vol. 2. New York, New York, USA: McGraw Hill; 2001:3063–3101.

3. Abnormal Sulfobromophthalein Metabolism in Rotor's Syndrome and Obligate Heterozygotes

4. 99mTc-HIDA cholescintigraphy in Dubin-Johnson and Rotor syndromes.

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