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Wilson’s disease: A review of what we have learned
Wilson’s disease (WD), which results from the defective ATP7B protein product, is characterized by impaired copper metabolism and its clinical consequences vary from an asymptomatic state to fulminant hepatic failure, chronic liver disease with or without cirrhosis, neurological, and psychiatric man...
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| Yayımlandı: | World J Hepatol |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Baishideng Publishing Group Inc
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4678372/ https://ncbi.nlm.nih.gov/pubmed/26692151 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4254/wjh.v7.i29.2859 |
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