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Insights into the management of Wilson’s disease
Wilson’s disease is a rare, inherited autosomal recessive disease of copper metabolism, in which the causative gene, ATP7B, results in absent or reduced function of the ATP7B transporter important for biliary excretion of copper and incorporation of copper into caeruloplasmin. Affected patients accu...
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| Publicado no: | Therap Adv Gastroenterol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5673017/ https://ncbi.nlm.nih.gov/pubmed/29147139 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1756283X17731520 |
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