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: Arnold, Jayantha, Sangwaiya, Arvind, Manglam, Vijay, Thursz, Mark, Beaumont, Caroline, Kannengiesser, Caroline, Busbridge, Mark
Formato: Artigo
Idioma:Inglês
Publicado: The WJG Press and Baishideng 2010
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Brief Article
Acceso en liña: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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