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Wilson disease—treatment perspectives
Wilson disease (WD) is a genetic disorder caused by pathological tissue copper accumulation with secondary damage of affected organs (mainly, but not limited to, the liver and brain). The main clinical symptoms of WD are, in concordance with the pathogenesis, hepatic and/or neuropsychiatric. Current...
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| Udgivet i: | Ann Transl Med |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
AME Publishing Company
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6531659/ https://ncbi.nlm.nih.gov/pubmed/31179305 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2018.12.09 |
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