1. Adams, P.C., Deugnier, Y., Moirand, R., and Brissot, P., The Relationship between Iron Overload, Clinical Symptoms and Age in 410 Patients with Hemochromatosis, Hepatology, 1997, vol. 25, pp. 162–166.
2. Bothwel, T.H., Charlton, R.W., Motulsky, A.G., et al., Hemochromatosis, The Metabolic and Molecular Bases of Inherited Disease, Scriver, C.R., Beaudet, A.L., Sly, W.S., and Valle, D., Eds., New York: McGraw-Hill, 1995, pp. 2237–2269.
3. Adams, P.C. and Valberg, L.S., Evolving Expression of Hereditary Hemochromatosis, Semin. Liver Dis., 1996, vol. 16, pp. 47–54.
4. Niederau, C., Fisher, R., Purshel, A., et al., Long-Term Survival in Patients with Hereditary Hemochromatosis, Gastroenterology, 1996, vol. 110, pp. 1107–1119.
5. Powell, L.W., Jazwinska, E., and Halliday, J.W., Primary Iron Overload, Iron Metabolism in Health and Disease, Brock, J.H., Halliday, J.W., Pippard, M.J., and Powell, L.W., Eds., London: Saunders, 1994, pp. 227–270.