Concepedia

A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes

Borut Peterlin, Mojca Globočnik Petrovič, Jana Makuc, Marko Hawlina, Daniel Petrovič

Journal of Human Genetics · 2003 · 31 citations · 16 references

DOI

Concepts

References

16

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

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The Wisconsin Epidemiologic Study of Diabetic Retinopathy

Ronald Klein · Archives of Ophthalmology · 1984 · 1.5K citations

, , +14

Crystal Structure of the Hemochromatosis Protein HFE and Characterization of Its Interaction with Transferrin Receptor

José Antonio Lebrón, M. J. Bennett, Daniel E. Vaughn et al. · Cell · 1998 · 647 citations · Full text

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The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression

John N. Feder, Zenta Tsuchihashi, Alivelu Irrinki et al. · Journal of Biological Chemistry · 1997 · 479 citations · Full text

, , +10

Evaluation of the iron status of a population

JD Cook, C. A. Finch, NJ Smith · Blood · 1976 · 469 citations · Full text

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