V. Gérolami, G. Le Gac, L. Mercier, M. Nezri, J-L. Bergé-Lefranc, C. Férec. Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent. haematol [Internet]. 2008Apr.30 [cited 2024Dec.22];93(5):e45-e46. Available from: https://haematologica.org/article/view/4866