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Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy
BACKGROUND: β Thalassemia is one of the most common groups of hereditary haemoglobinopathies. Affected people with thalassemia major are dependent on regular blood transfusion which on the long term leads to iron overload. Hepcidin is a peptide hormone and an important regulator of iron homeostasis,...
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| Pubblicato in: | BMC Med Genet |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7140315/ https://ncbi.nlm.nih.gov/pubmed/32268883 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01011-3 |
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