Transferrin Receptor Mutation Analysis in Hereditary Hemochromatosis Patients

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

John N. Feder, Andreas Gnirke, Zenta Tsuchihashi et al. · Nature Genetics · 1996 · 3.7K citations

Life Sciences, Genetics, Molecular Genetics +12

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

John N. Feder, David M. Penny, Alivelu Irrinki et al. · Proceedings of the National Academy of Sciences · 1998 · 838 citations

Life Sciences, Genetics, Molecular Biology +15

Global prevalence of putative haemochromatosis mutations.

Alison T. Merryweather‐Clarke, J. J. Pointon, Jeremy D. Shearman et al. · Journal of Medical Genetics · 1997 · 794 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Mutation Analysis in Hereditary Hemochromatosis

Ernest Beutler, Terri Gelbart, Carol West et al. · Blood Cells Molecules and Diseases · 1996 · 427 citations

Life Sciences, Genetics, Molecular Genetics +14

Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis

Seppo Parkkila, Abdül Waheed, Robert S. Britton et al. · Proceedings of the National Academy of Sciences · 1997 · 345 citations

Medicine, Genetics, Molecular Genetics +17