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Biomarkers for diagnosis of Wilson's disease
BACKGROUND: Wilson's disease, first described by Samuel Wilson in 1912, is an autosomal recessive metabolic disorder resulting from mutations in the ATP7B gene. The disease develops as a consequence of copper accumulating in affected tissues. There is no gold standard for the diagnosis of Wilso...
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| Publicado en: | Cochrane Database Syst Rev |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley & Sons, Ltd
2019
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6953362/ https://ncbi.nlm.nih.gov/pubmed/31743430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD012267.pub2 |
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