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Wilson's disease: Revisiting an old friend
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and secondly in other organs, such as the central nervous system. It is a hereditary autosomal recessive disease caused by a deficiency in the ATP7B transporter. This protein facilitates the incorpora...
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| Publicado no: | World J Hepatol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8239488/ https://ncbi.nlm.nih.gov/pubmed/34239699 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4254/wjh.v13.i6.634 |
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