References
- Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, et al. A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis. Nat Genet 1996;13:399–408.
- Edwards CQ, Griffen LM, Goldgar D, Drummond C, Skolnick MH, Kushner JP. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors. N Engl J Med 1988;318:1355–62.
- Phatak P, Sham R, Rabuertas R, Dunnigan K, O’Leary M, Braggins C, et al. Prevalence of hereditary hemochromatosis in a sample of 16,031 primary care patients. Ann Intern Med 1998;129: 954–61.
- Niederau C, Niederau CM, Lange S, Littauer A, Abdel-Jalil N, Maurer M, et al. Screening for hemochromatosis and iron deficiency in employees and primary care patients in Western Germany. Ann Intern Med 1998;128:337–45.
- Adams PC, Valberg LS. Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping. Am J Gastroenterol 1999; 94:1593–600.
- Guyader D, Jacquelinet C, Moirand R, Turlin B, Mendler M, Chaperon J, et al. Non-invasive prediction of fibrosis in C282Y homozygous hemochromatosis. Gastroenterology 1998;115:929–36.
- Adams PC. Non-expressing C282Y homozygotes for hemochromatosis: minority or majority of cases? Mol Genet Metab 2000;71:81–6.
- Adams PC, Brissot P, Pietrangelo A, Powell LW. EASL Consensus conference on haemochromatosis. J Hepatol 2000;33:485–505.
- Olynyk J, Cullen D, Aquilia S, Rossi E, Summerville L, Powell LW. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med 1999;341:718–24.
- Seeff L, Miller R, Rabkin C, Buskell-Bales Z, Straley-Eason K, Smoak B, et al. 45-year follow-up of hepatitis C virus infection in healthy young adults. Ann Intern Med 2000;132: 105–11.