Title : Rare causes of hereditary iron overload.

Pub. Date : 2002 Oct

PMID : 12382200






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Homozygous defects in a recently identified gene encoding transferrin receptor 2 lead to iron overload (hemochromatosis type 3) with symptoms similar to those seen in patients with HFE-associated hereditary hemochromatosis (hemochromatosis type 1). Iron transferrin receptor 2 Homo sapiens