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Hepatocyte GP73 expression in Wilson disease

BACKGROUND/AIMS: Wilson disease (WD) is a disorder of copper transport caused by mutations within the ATP7B gene. WD is phenotypically variable and can present with predominantly hepatic or neurologic manifestations. The mechanisms responsible for this variability are unknown. GP73, a Golgi membrane...

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Hlavní autoři: Wright, Lorinda M., Huster, Dominik, Lutsenko, Svetlana, Wrba, Fritz, Ferenci, Peter, Fimmel, Claus J.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2009
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2750828/
https://ncbi.nlm.nih.gov/pubmed/19596473
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jhep.2009.05.029
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