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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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| Опубликовано в: : | J Neurochem |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2018
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| Предметы: | |
| Online-ссылка: | 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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