Ka, C., Guellec, J., Pepermans, X., Kannengiesser, C., Ged, C., Wuyts, W., Cassiman, D., de Ledinghen, V., Varet, B., de Kerguenec, C., Oudin, C., Gourlaouen, I., Lefebvre, T., Férec, C., Callebaut, I. and Le Gac, G. (2018) “The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism”, Haematologica. Pavia, Italy, 103(11), pp. 1796-1805. doi: 10.3324/haematol.2018.189845.