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Modifying factors and phenotypic diversity in Wilson’s disease
Wilson’s disease (WD) is a human disorder of copper homeostasis caused by mutations in the copper-transporting ATPase ATP7B. WD is characterized by copper accumulation, predominantly in the liver and brain; hepatic pathology; and wide differences between patients in the age of onset and the spectrum...
Bewaard in:
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4083489/ https://ncbi.nlm.nih.gov/pubmed/24702697 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nyas.12420 |
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