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Description
J Histochem Cytochem 54:201213
Etiology Primary (hereditary) hemochromatosis Classical and most frequent form: adult hemochromatosis type I Homozygous or heterozygous for the HFE gene defect Located on chromosome 6 Most commonly affects C282Y and H63D Associated with HLA-A3 genotype Inheritance: autosomal recessive with incomplete penetrance Further forms: Hemochromatosis types IIIV are also hereditary, but significantly less frequent
[DOI] [PMC free article] [PubMed] [Google Scholar] 56.Ahmed M.A., Muntingh G., Rheeder P
Ranaut, A., Khandnor, P
