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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...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2000
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| Gaiak: | |
| Sarrera elektronikoa: | 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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