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Intestinal expression of metal transporters in Wilson’s disease
In Wilson’s disease (WND), biallelic ATP7B gene mutation is responsible for pathological copper accumulation in the liver, brain and other organs. It has been proposed that copper transporter 1 (CTR1) and the divalent metal transporter 1 (DMT1) translocate copper across the human intestinal epitheli...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer Netherlands
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3825560/ https://ncbi.nlm.nih.gov/pubmed/23963605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10534-013-9668-5 |
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