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The Function of ATPase Copper Transporter ATP7B in Intestine
BACKGROUND & AIMS: Wilson disease is a disorder of copper (Cu) misbalance caused by mutations in the ATPase copper transporting beta gene (ATP7B). ATP7B is highly expressed in the liver—the major site of Cu accumulation in patients with Wilson disease. The intestine also expresses ATP7B, but lit...
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| 出版年: | Gastroenterology |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5848507/ https://ncbi.nlm.nih.gov/pubmed/28958857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.gastro.2017.09.019 |
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