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Ramos Sousa
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Changes in Erythropoiesis in Type 3 Hemochromatosis Mouse Models
Type 3 haemochromatosis is a rare inherited iron excess condition that results in organ dysfunction. Mutations in the transferrin receptor 2 gene, which codes for two major isoforms, cause HFE3. Tfr2 is a hepatic regulator of the iron inhibitor hepcidin. Tfr2 is an intracellular isoform of the protein that controls iron levels in reticuloendothelia... Read More»
: J Mol Pharm Org Process Res 2023, 11:174
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