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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Detalles Bibliográficos
Autores principales: Seessle, Jessica, Gohdes, Annina, Gotthardt, Daniel Nils, Pfeiffenberger, Jan, Eckert, Nicola, Stremmel, Wolfgang, Reuner, Ulrike, Weiss, Karl Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127787/
https://www.ncbi.nlm.nih.gov/pubmed/21595966
http://dx.doi.org/10.1186/1476-511X-10-83

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127787/
https://www.ncbi.nlm.nih.gov/pubmed/21595966
http://dx.doi.org/10.1186/1476-511X-10-83

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