van de Steeg, E., Stránecký, V., Hartmannová, H., Nosková, L., Hřebíček, M., Wagenaar, E., . . . Schinkel, A. H. (2012). Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver. American Society for Clinical Investigation.
Chicago-stil citatvan de Steeg, Evita, et al. Complete OATP1B1 and OATP1B3 Deficiency Causes Human Rotor Syndrome By Interrupting Conjugated Bilirubin Reuptake Into the Liver. American Society for Clinical Investigation, 2012.
MLA-referensvan de Steeg, Evita, et al. Complete OATP1B1 and OATP1B3 Deficiency Causes Human Rotor Syndrome By Interrupting Conjugated Bilirubin Reuptake Into the Liver. American Society for Clinical Investigation, 2012.
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