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HJV and HFE Play Distinct Roles in Regulating Hepcidin
Aims: Hereditary hemochromatosis (HH) is an iron overload disease that is caused by mutations in HFE, HJV, and several other genes. However, whether HFE-HH and HJV-HH share a common pathway via hepcidin regulation is currently unclear. Recently, some HH patients have been reported to carry concurren...
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| Pubblicato in: | Antioxid Redox Signal |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Mary Ann Liebert, Inc.
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4410569/ https://ncbi.nlm.nih.gov/pubmed/25608116 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/ars.2013.5819 |
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