REFERENCES
- Galanello R, Turco M P, Barella S, et al. Iron storse and iron deficiency in children heterozygous for β thalassemia. Haematology 1990; 75: 319–322
- Merryweather-Clarke A T, Shearman J D, Pointon J J, Robson K J. Global prevalence of putative hemochromatosis mutations. J Med Genet 1997; 34: 275–278, [PUBMED], [INFOTRIEVE], [CSA]
- Feder J N, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat genet 1996; 13: 399–408, [PUBMED], [INFOTRIEVE], [CROSSREF]
- Camaschella C, De Gobbi M, Roetto A. Hereditary hemochromatosis: progress and perspectives. Rev Clin Exp Hematol 2000; 4.4: 302–321, [CROSSREF]
- Restagno G, Gomez A M, Sbaiz L, et al. A pilot C282 Y hemochromatosis screening in Italian newborns by TaqMan technology. Genet Testing 2000; 4: 177–181, [CROSSREF], [CSA]
- Cassanelli S, Pignatti E, Montosi G, et al. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healty adult population in Italy. J Hepatol 2001; 34: 523–528, [PUBMED], [INFOTRIEVE], [CROSSREF]
- Girouard J, Giguere Y, Delage R. Rousseau F. Prevalence of the HFE gene C282Y and H63D mutations in a French-Canadian population of neonates and in referred patients. Hum Mol Genet 2002; 11: 185–189, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Piperno A, Mariani R, Arosio C, et al. Hemochromatosis in patients with β-thalasaemia trait. Br J Haematol 2000; 11: 908–914, [CROSSREF]
- Melis M A, Cau M, Deidda F, Bartella S, Cao A. Galanello R. H63D mutation in HFE gene increases iron overload in β-thalassemia carriers. Hematology 2002; 87: 242–245
- Riva A, Mariani R, Bovo G, et al. Type 3 hemocromatosis and β-thalassemia trait. Eur J Haematol 2004; 72: 370–374, [PUBMED], [INFOTRIEVE], [CROSSREF]
- Arruda V R, Agostinho M F, Cancado R, Costa F F, Saad STO. β-Thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene. Am J Hematol 2000; 63: 230, [PUBMED], [INFOTRIEVE], [CROSSREF]