Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12185-013-1338-4.pdf
Reference17 articles.
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2. Heimpel H, Kellermann K, Neuschwander N, Högel J, Schwarz K. The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells. Haematologica. 2010;95:1034–6.
3. Greiner TC, Burns CP, Dick FR, Henry KM, Mahmood I. Congenital dyserythropoietic anemia type II diagnosed in a 69-year-old patient with iron overload. Am J Clin Pathol. 1992;98:522–5.
4. Iolascon A, Delaunay J, Wickramasinghe SN, Perrotta S, Gigante M, Camaschella C. Natural history of congenital dyserythropoietic anemia type II. Blood. 2001;98:1258–60.
5. Kamiya T, Manabe A. Congenital dyserythropoietic anemia. Int J Hematol. 2010;92:432–8.
Cited by 3 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
1. Congenital dyserythropoiesis anemia type Ia with a novel CDAN1 mutation diagnosed by whole exome sequencing;Molecular Genetics & Genomic Medicine;2020-03-11
2. The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type I;British Journal of Haematology;2019-03-05
3. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia;International Journal of Hematology;2018-06-23
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