1.
Gérolami V, Le Gac G, Mercier L, Nezri M, Bergé-Lefranc J-L, Férec C. Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent. Haematologica 2008; 93(5):e45-e46; https://doi.org/10.3324/haematol.12884.