CareLit · DOI-Nachweis · Zeitschrift für Gastroenterologie
Localization of the Wilson disease protein in murine intestine
DOI 10.1055/s-0028-1089422
Bibliografische Angaben
Nachweis in CareLit
Autor:innenKH Weiss, D Gotthardt, J Wurz, U Merle, W Stremmel, J Füllekrug
ZeitschriftZeitschrift für Gastroenterologie
Ausgabe09/2008
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Wilson disease is an inherited disorder of human copper metabolism, characterized by accumulation of copper, predominantly liver and brain. The gene defect lies in the Wilson disease protein ATP7B, a copper transporting ATPase highly active in hepatocytes. In the liver ATP7B is essential for excretion of excess copper into the bile and for copper loading of ceruloplasmin in the Golgi apparatus. The extrahepatic role…
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Zitierempfehlung
KH Weiss, D Gotthardt, J Wurz, U Merle, W Stremmel, J Füllekrug (2008) Localization of the Wilson disease protein in murine intestine. Zeitschrift für Gastroenterologie (09). https://doi.org/10.1055/s-0028-1089422
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