New Codanin-1 Gene Mutations in a Italian Patient with Congenital Dyserythropoietic Anemia Type I and Heterozygous Beta-Thalassemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-015-0633-z.pdf
Reference12 articles.
1. Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H et al (2002) Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1. Am J Hum Genet 71:1467–1474
2. Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W et al (2009) Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nat Genet 41:936–940
3. Liljeholm M, Irvine AF, Wikberg AL, Norberg A, Month S, Sandström H et al (2013) Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23. Blood 121(23):4791–4799
4. Wickramasinghe SN (1997) Dyserythropoiesis and congenital dyserythropoietic anemias. Br J Haematol 98:785–797
5. Tamary H, Shalev H, Luria D, Shaft D, Zoldan M, Shalmon L et al (1996) Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I. Blood 87:1763–1770
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