Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome

[1] Hyperferritinaemia in the absence of iron overload. [J]. GUT, 1997, 41 (03) : 408 - 410

[2] Genetic and clinical description of hemochromatosis probands and heterozygotes: Evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis [J]. BLOOD CELLS MOLECULES AND DISEASES, 1997, 23 (08) : 135 - 145

[3] BARTON JC, 1991, HOSP PRACT, V26, P46

[4] MUTATION IN THE IRON-RESPONSIVE ELEMENT OF THE L-FERRITIN MESSENGER-RNA IN A FAMILY WITH DOMINANT HYPERFERRITINEMIA AND CATARACT [J]. NATURE GENETICS, 1995, 11 (04) : 444 - 446

[5] Beutler Ernest, 1996, Blood Cells Molecules and Diseases, V22, P187, DOI 10.1006/bcmd.1996.0027

[6] USEFULNESS AND LIMITATIONS OF LABORATORY AND HEPATIC IMAGING STUDIES IN IRON-STORAGE DISEASE [J]. GASTROENTEROLOGY, 1990, 99 (04) : 1079 - 1091

[7] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [J]. NATURE GENETICS, 1996, 13 (04) : 399 - 408

[8] A point mutation in the bulge of the iron-responsive element of the L ferritin gene in two families with the hereditary hyperferritinemia-cataract syndrome [J]. BLOOD, 1998, 91 (01) : 319 - 323

[9] A new syndrome of liver iron overload with normal transferrin saturation [J]. LANCET, 1997, 349 (9045) : 95 - 97

[10] Hereditary hemochromatosis [J]. CLINICA CHIMICA ACTA, 1996, 245 (02) : 139 - 200

[1] Hyperferritinaemia in the absence of iron overload. [J]. GUT, 1997, 41 (03) : 408 - 410

[2] Genetic and clinical description of hemochromatosis probands and heterozygotes: Evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis [J]. BLOOD CELLS MOLECULES AND DISEASES, 1997, 23 (08) : 135 - 145

[3] BARTON JC, 1991, HOSP PRACT, V26, P46

[4] MUTATION IN THE IRON-RESPONSIVE ELEMENT OF THE L-FERRITIN MESSENGER-RNA IN A FAMILY WITH DOMINANT HYPERFERRITINEMIA AND CATARACT [J]. NATURE GENETICS, 1995, 11 (04) : 444 - 446

[5] Beutler Ernest, 1996, Blood Cells Molecules and Diseases, V22, P187, DOI 10.1006/bcmd.1996.0027

[6] USEFULNESS AND LIMITATIONS OF LABORATORY AND HEPATIC IMAGING STUDIES IN IRON-STORAGE DISEASE [J]. GASTROENTEROLOGY, 1990, 99 (04) : 1079 - 1091

[7] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [J]. NATURE GENETICS, 1996, 13 (04) : 399 - 408

[8] A point mutation in the bulge of the iron-responsive element of the L ferritin gene in two families with the hereditary hyperferritinemia-cataract syndrome [J]. BLOOD, 1998, 91 (01) : 319 - 323

[9] A new syndrome of liver iron overload with normal transferrin saturation [J]. LANCET, 1997, 349 (9045) : 95 - 97

[10] Hereditary hemochromatosis [J]. CLINICA CHIMICA ACTA, 1996, 245 (02) : 139 - 200