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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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Bibliografiske detaljer
Main Authors: Weiss, Karl Heinz, Wurz, Judith, Gotthardt, Daniel, Merle, Uta, Stremmel, Wolfgang, Füllekrug, Joachim
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Science Inc 2008
Fag:
Online adgang: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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