Iron deficiency disorders

Montosi G, Donovan A, Totaro A et al. (2001) Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. Journal of Clinical Investigation, 108, 619-623.

Roetto A., Papanikolaou G, Politou M et al. (2002) Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis. Nature Genetics, epub ahead of print.

Roy CN, Andrews NC. (2001) Recent advances in disorders of iron metabolism: mutations, mechanisms and modifiers. Human Molecular Genetics, 10, 2181-2186.

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