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

AuthorsSilvia Majore, Bianca Maria Ricerca, Francesca Clementina Radio, Francesco Binni, Ilaria Cosentino, Giulia Gallusi, Carmelilia De Bernardo, Aldo Morrone, Paola Grammatico
JournalBlood cells, molecules & diseases (Blood Cells Mol Dis) Vol. 50 Issue 1 Pg. 31-2 (Jan 2013) ISSN: 1096-0961 [Electronic] United States
PMID22981443 (Publication Type: Case Reports, Letter)
Chemical References
  • Receptors, Transferrin
  • TFR2 protein, human
Topics
  • Africa South of the Sahara
  • Amino Acid Sequence
  • Anemia, Sideroblastic (genetics)
  • DNA Mutational Analysis
  • Hemochromatosis (genetics, pathology)
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Mutation
  • Receptors, Transferrin (deficiency, genetics)
  • Sequence Alignment

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