Author:
Casanovas Guillem,Swinkels Dorine W.,Altamura Sandro,Schwarz Klaus,Laarakkers Coby M.,Gross Hans-Juergen,Wiesneth Markus,Heimpel Hermann,Muckenthaler Martina U.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Drug Discovery,Molecular Medicine
Reference25 articles.
1. Wickramasinghe SN, Wood WG (2005) Advances in the understanding of the congenital dyserythropoietic anaemias. Br J Haematol 131:431–446
2. Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Cretien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rossler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H (2002) Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1. Am J Hum Genet 71:1467–1474
3. Iolascon A, D'Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice B (1996) Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects. Haematologica 81:543–559
4. Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H (2009) Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nat Gen 41:936–940
5. Andrews NC (2008) Forging a field: the golden age of iron biology. Blood 112:219–230
Cited by
41 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献