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Alterations of lipid metabolism in Wilson disease

INTRODUCTION: Wilson disease (WD) is an inherited disorder of human copper metabolism, characterised by accumulation of copper predominantly in the liver and brain, leading to severe hepatic and neurological disease. Interesting findings in animal models of WD (Atp7b(-/- )and LEC rats) showed altere...

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Bibliografische gegevens
Hoofdauteurs: Seessle, Jessica, Gohdes, Annina, Gotthardt, Daniel Nils, Pfeiffenberger, Jan, Eckert, Nicola, Stremmel, Wolfgang, Reuner, Ulrike, Weiss, Karl Heinz
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2011
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3127787/
https://ncbi.nlm.nih.gov/pubmed/21595966
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1476-511X-10-83
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