טוען...
Elevated copper impairs hepatic nuclear receptor function in Wilson’s disease
Wilson’s disease (WD) is an autosomal recessive disorder that results in accumulation of copper in the liver as a consequence of mutations in the gene encoding the copper-transporting P-type ATPase (ATP7B). WD is a chronic liver disorder, and individuals with the disease present with a variety of co...
שמור ב:
| הוצא לאור ב: | J Clin Invest |
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| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4588285/ https://ncbi.nlm.nih.gov/pubmed/26241054 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI78991 |
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