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Nature Reviews Disease Primers article: Wilson disease
Wilson disease (WD) is a potentially treatable, inherited disorder of copper metabolism characterised by pathological copper accumulation. WD is caused by mutations in the ATP7B gene, which encodes a transmembrane copper-transporting ATPase, leading to copper overload in the liver, brain and other o...
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| 發表在: | Nat Rev Dis Primers |
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| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6416051/ https://ncbi.nlm.nih.gov/pubmed/30190489 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41572-018-0018-3 |
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