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HEMOCHROMATOSIS, TYPE 3

Known as: HEMOCHROMATOSIS DUE TO DEFECT IN TRANSFERRIN RECEPTOR 2, HFE3 
National Institutes of Health

Related topics

Related topics

5 relations

Broader (2)

HemochromatosisTransferrin Receptor
TFR2 geneTFR2 wt AlleleTFR2, MET172LYS

Papers overview

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2001
2001
Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.
Hereditary hemochromatosis (HH) is a genetically heterogeneous disease. The HFE gene resides on chromosome 6 and its mutations… 
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