Elevated copper impairs hepatic nuclear receptor function in Wilson’s disease

Wilson’s disease (WD) is an autosomal recessive disorder that results in accumulation of copper in the liver as a consequence of mutations in the gene encoding the copper-transporting P-type ATPase (ATP7B). WD is a chronic liver disorder, and individuals with the disease present with a variety of co...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Wooton-Kee, Clavia Ruth, Jain, Ajay K., Wagner, Martin, Grusak, Michael A., Finegold, Milton J., Lutsenko, Svetlana, Moore, David D.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2015
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4588285/
https://ncbi.nlm.nih.gov/pubmed/26241054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI78991
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