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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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Detalhes bibliográficos
Main Authors: Gaffney, D, Fell, G, O'Reilly, D
Formato: Artigo
Idioma:Inglês
Publicado em: 2000
Assuntos:
Acesso em linha: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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