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pubmed-article:21269740pubmed:dateCreated2011-5-23lld:pubmed
pubmed-article:21269740pubmed:abstractTextWilson's disease (WD) is an inherited disorder of copper metabolism, characterized by the accumulation of copper in the body due to defective biliary copper excretion by hepatocytes. We report a series of 19 patients with WD.lld:pubmed
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pubmed-article:21269740pubmed:copyrightInfoCopyright © 2010 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.lld:pubmed
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pubmed-article:21269740pubmed:volume32lld:pubmed
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pubmed-article:21269740pubmed:year2011lld:pubmed
pubmed-article:21269740pubmed:articleTitle[Wilson's disease in an adult].lld:pubmed
pubmed-article:21269740pubmed:affiliationService de médecine interne orientée vers les maladies orphelines et systémiques, hôpitaux de Brabois, CHU de Nancy, rue du Morvan, Vandœuvre, France.lld:pubmed
pubmed-article:21269740pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21269740pubmed:publicationTypeEnglish Abstractlld:pubmed