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Advance in the pathogenesis and treatment of Wilson disease
Wilson disease is an autosomal recessive disorder of copper metabolism. Diagnosis depends primarily on clinical features, biochemical parameters and the presence of the Kayser-Fleischer ring. Genetic analysis for mutations within ATP7B is a convincing diagnostic tool. The traditional treatment for W...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3526418/ https://ncbi.nlm.nih.gov/pubmed/23210912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2047-9158-1-23 |
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