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Wilson's disease: acute and presymptomatic laboratory diagnosis and monitoring
Wilson's disease, the most common inherited disorder of copper metabolism, is a recessive genetic condition. The clinical presentation of Wilson's disease is very variable. It is characterised by low serum copper and caeruloplasmin concentrations coupled with the pathological accumulation...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2000
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1731102/ https://ncbi.nlm.nih.gov/pubmed/11127261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jcp.53.11.807 |
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