4Iolascon A, Russo R, Esposito MR, et al. Molecular analysis of 42 patients with congenital dyserythropoietic anemia type Il : new mutations in the SEC23B gene and a search for a genotype.phenotype relationship. Haematologica, 2010, 95:708-715.
5Liu G, Niu S, Dong A, et al. A Chinese family carrying novel mutations in SEC23B and HFE2, the genes responsible for con.genital dyserythropoietic anaemia n (CDA ll ) and primary iron overload, respectively. BrJ Haematol, 2012,158:143-145.
6Bansal SS, HalketJM, FusovaJ, et al. Quantification ofhepcidin using matrix- assisted laser desorption/ionization time- of- flight mass spectrometry. Rapid Commun Mass Spectrom, 2009, 23: 1531-1542.
7Wickramasinghe SN, Wood WG. Advances in the understanding of the congenital dyserythropoietic anaemias. BrJ Haematol, 2005, 131 :431-446.
9Schwarz K, lolascon A, Verissimo F, et al. Mutations affecting the secretory COPIl coat component SEC23B cause congenital dyserythropoietic anemia type n. Nat Genet, 2009, 41 :936-940.
10Casanovas G, Swinkels DW, A1tamura S, et al. Growth differen.tiation factor 15 in patients with congenital dyserythropoietic anaemia (CDA) type n.J Mol Med (Berl), 2011, 89:811-816.
