1. Feder JN, Gnirke A, Tomas W, Tsuchiashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Rish NJ, Bacon BR, Wolff RK: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics 1996; 13: 399-408.
2. Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Pilip Morris C, Walsh TP: Haemochromatosis and HLA-H. Nature Genetics 1996; 14: 249-251.
3. Jouanolle AM, Gandon G, Jezequel P, Blayau M, Campion ML, Yaouang J, Mosser J, Fergelot P, Chauvel B, Bouric P, Carn G, Andrieux N, Gicquel I, Le Gall JY, David V: Haemochromatosis and HLA-H. Nature Genetics 1996; 14: 251-252.
4. Barton JC, Bertoli LF: Haemochromatosis: The genetic disorder of the twenty-first century. Nature Medicine 1996; 2: 394-395.
5. Brissot P: Le diagnostic de l'hemochromatose a l'heure du test genetique. La Presse Medicale 2000; 29: 425-427.
6. Burke W, Thomson E, Khoury MJ, McDonnell M, Press N, Adams PC, Barton JC, Beutler E, Brittenham G, Buchanan A, Clayton EW, Cogswell ME, Meslin EM, Motulsky AG, Powell LW, Sigal E, Wilfond BS, Collins FS: Hereditary hemochromatosis, gene discovery and its implications for population-based screening. JAMA 1998; 280: 172-178.
7. Beutler E: Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations. The Lancet 1997; 349: 296-297.
8. Mura C, Raguenes O, Ferec C: HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis. Blood 1999; 93: 2502-2505.
9. Hansen EH, Imperatore G, Burke W: HFE gene and hereditary hemochromatosis: a HuGe review. Am J Epidemiol 2001; 154: 193-206.
10. Simonsen K, Dissing , Rudbeck L, Schwartz M: Rapid and simple determination of hereditary hemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutation. Ann Hum Genet 1999; 63: 193-197.
11. Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT: Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands. Blood Cells Mol Dis 1999; 25: 147-155.
12. Towner P. Isolation of DNA by SDS-proteinase K treatment. In: Essential Molecular Biology, Vol. 1, Brown TA, (ed). Oxford University Press Inc., New York, NY, USA, 1995; 52-53.
13. Martinez PA, Jeanjean Ph, Masmejean C, Guillard A, Biron C, Rabesandratana H, Schved JF: Simple and rapid detection of the newly described mutations in the HLA-H gene. Blood 1997; 89: 1835-1836.
14. Merryweather-Clarke A, Shearman JD, Robson KJH, Pointon JJ, Liu YT, Bomford A, Dooley J, Walker AP, Worwood M: Hemochromatosis-related mutation detection. Blood 1998; 91: 2620-2621.
15. Lynas C: A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis. Blood 1997; 90: 4235-4236.
16. Hemochromatosis; HFE. Online Mendelian Inheritance In Men-entry *235200. http://www.ncbi.nlm.nih. gov/htbin-post/Omim/