C. Prass

HFE gene knockout produces mouse model of hereditary hemochromatosis.

W. Sly, B. Bacon, D. Ruddy, 1998, Proceedings of the National Academy of Sciences of the United States of America.

A Robust Immunohistochemical Assay for Detecting PTEN Expression in Human Tumors

J. Lanchbury, S. Stone, C. Prass, 2011, Applied immunohistochemistry & molecular morphology : AIMM.

Hereditary hemochromatosis in liver transplantation.

R. Wolff, B. Bacon, T. Schiano, 1999, Liver transplantation and surgery : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

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

R. Wolff, W. Sly, F. Mapa, 1997, The Journal of Biological Chemistry.

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

M. C. Ellis, A. Gnirke, N. Risch, 1996, Nature Genetics.

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.

D J Lockhart, R. Mei, D. Lockhart, 2000, Genome research.

Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22.

A. Gnirke, R. Wolff, C. Prass, 1997, Genome research.