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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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Autori principali: Wright, Lorinda M., Huster, Dominik, Lutsenko, Svetlana, Wrba, Fritz, Ferenci, Peter, Fimmel, Claus J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2009
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Accesso online: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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