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A systems approach implicates nuclear receptor targeting in the Atp7b(−/−) mouse model of Wilson’s Disease
Wilson’s disease (WD) is an inherited disorder of copper metabolism characterized by liver disease and/or neurologic and psychiatric pathology. The disease is a result of mutation in ATP7B, which encodes the ATP7B copper transporting ATPase. Loss of copper transport function by ATP7B results in copp...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3695828/ https://ncbi.nlm.nih.gov/pubmed/22565294 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c2mt20017a |
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