Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis. by Merryweather-Clarke, A, Cadet, E, Bomford, A, Capron, D, Viprakasit, V, Miller, A, McHugh, P, Chapman, R, Pointon, J, Wimhurst, V, Livesey, K, Tanphaichitr, V, Rochette, J, Robson, K

A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis. by Cadet, E, Capron, D, Perez, A, Crépin, SN, Arlot, S, Ducroix, J, Dautréaux, M, Fardellone, P, Leflon, P, Merryweather-Clarke, A, Livesey, K, Pointon, J, Rose, P, Harcourt, J, Emery, J, Sueur, J, Feyt, R, Robson, K, Rochette, J

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience by Robson, K, Merryweather-Clark, A, Pointon, J, Shearman, J, Halsall, D, Kelly, A, Cox, T, Rosenberg, WM, Howell, M, Eccles, D, Patch, C, Fowler, A, Wallace, D, Camaschella, C, Roetto, A, Zecchina, G, De Gobbi, M, Gasparini, P, Cadet, E, Vandwalle, J, Capron, D, Rochette, J, Borot, N, Demangel, C, Dery, R