Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene-Reference-Cited by-同舟云学术

Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene

Published:2008-06-25 Issue:9 Volume:87 Page:751-754
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Ru Yong Xi,Zhu Xiao-fan,Yan Wen-wei,Gao Jing-tao,Schwarz Klaus,Heimpel Hermann

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-008-0519-3.pdf

Reference23 articles.

1. Ahmed MR, Zaki M, Sabry MA, Higgs D, Vyas P, Wood WG et al (2006) Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I. Br J Haematol 133:444–445, doi: 10.1111/j.1365-2141.2006.06089.x

2. Bader-Meunier B, Leverger G, Tchernia G, Schischmanoff O, Cynober T, Bernaudin F et al (2005) Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children. J Pediatr Hematol Oncol 27:416–419, doi: 10.1097/01.mph.0000175406.42427.c9

3. 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, doi: 10.1086/344781

4. Ghosh K, Mohanty D, Bhagwat AG, Das KC (1985) Congenital dyserythropoietic anaemia (CDA) type I-a case report with ultrastructural study. Folia Haematol (Frankf) 112:716–722

5. Goede JS, Benz R, Fehr J, Schwarz K, Heimpel H (2006) Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy. Ann Hematol 85:591–595, doi: 10.1007/s00277-006-0143-z

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