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Hepcidin levels in hereditary hyperferritinemia: Insights into the iron-sensing mechanism in hepatocytes
AIM: To study the role of hepcidin in hereditary hyperferritinemia cataract syndrome (HHCS). METHODS: Six patients from two families with HHCS, confirmed by genetic analysis showing A to G mutation at position +40 in the L-ferritin gene, were recruited to undergo serum hepcidin and prohepcidin measu...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The WJG Press and Baishideng
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2909553/ https://ncbi.nlm.nih.gov/pubmed/20653062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v16.i28.3541 |
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