Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction?

MeSH terms

• Africa South of the Sahara
• Amino Acid Sequence
• Anemia, Sideroblastic / genetics*
• DNA Mutational Analysis
• Hemochromatosis / genetics*
• Hemochromatosis / pathology
• Heterozygote
• Humans
• Male
• Middle Aged
• Molecular Sequence Data
• Mutation
• Receptors, Transferrin / deficiency
• Receptors, Transferrin / genetics*
• Sequence Alignment