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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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| Publicado no: | Gastroenterology |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | 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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