Clinical haemochromatosis in HFE mutation carriers. by Cox, T, Rochette, J, Camaschella, C, Walker, A, Robson, K

Molecular Basis of Phenylketonuria in Italy by Dianzani I., Camaschella C., Ferrero G. B., De Sanctis L., Ponzone A., Cotton R. G. H.

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A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. by Roetto, A, Merryweather-Clarke, A, Daraio, F, Livesey, K, Pointon, J, Barbabietola, G, Piga, A, Mackie, P, Robson, K, Camaschella, C

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. by Roetto, A, Merryweather-Clarke, A, Daraio, F, Livesey, K, Pointon, J, Barbabietola, G, Piga, A, Mackie, P, Robson, K, Camaschella, C

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