Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent - V. Gérolami; G. Le Gac; L. Mercier; M. Nezri; J-L. Bergé-Lefranc; C. Férec (Haematologica, 2008)