The authors report the case of two patients with secondary hemochromatosis in whom a C282Y mutation in the heterozygotic form was observed. They discuss the potential relationship between secondary hemochromatosis and the presence of the genetic abnormality.
Paris, I., Dahan, K., van Ypersele, M., Rahier, J., Michaux, L., & Buysschaert, M. (1999). Existe-t-il un lien entre hémochromatose secondaire et génétique? A propos de deux cas. Acta Clinica Belgica (Multilingual Edition), 54(1), 26-29. https://hdl.handle.net/2078.5/130495 (Original work published 1999)