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Animal models of Wilson disease

Wilson disease (WD) is an autosomal recessive disorder of copper metabolism manifesting with hepatic, neurological and psychiatric symptoms. The limitations of the currently available therapy for WD (particularly in the management of neuropsychiatric disease), together with our limited understanding...

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Bibliographic Details
Published in:J Neurochem
Main Authors: Reed, Emily, Lutsenko, Svetlana, Bandmann, Oliver
Format: Artigo
Language:Inglês
Published: 2018
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6107386/
https://ncbi.nlm.nih.gov/pubmed/29473169
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jnc.14323
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