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Localization of the Wilson disease protein in murine intestine
Wilson disease is an inherited disorder of human copper metabolism, characterized by gradual accumulation of copper in tissues, predominantly liver and brain. The gene defect lies in the Wilson disease protein ATP7B, a copper transporting ATPase highly active in hepatocytes. In the liver, ATP7B is e...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2732049/ https://ncbi.nlm.nih.gov/pubmed/18673401 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7580.2008.00954.x |
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