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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Detalles Bibliográficos
Autores principales: Wu, Fei, Wang, Jing, Pu, Chunwen, Qiao, Liang, Jiang, Chunmeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394540/
https://www.ncbi.nlm.nih.gov/pubmed/25803104
http://dx.doi.org/10.3390/ijms16036419

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394540/
https://www.ncbi.nlm.nih.gov/pubmed/25803104
http://dx.doi.org/10.3390/ijms16036419

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