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Wilson’s Disease: A Comprehensive Review of the Molecular Mechanisms
Wilson’s disease (WD), also known as hepatolenticular degeneration, is an autosomal recessive inherited disorder resulting from abnormal copper metabolism. Reduced copper excretion causes an excessive deposition of the copper in many organs such as the liver, central nervous system (CNS), cornea, ki...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4394540/ https://ncbi.nlm.nih.gov/pubmed/25803104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms16036419 |
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