Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23-Reference-Cited by-同舟云学术

Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23

Published:2013-06-06 Issue:23 Volume:121 Page:4791-4799
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Liljeholm Maria¹,Irvine Andrew F.²,Vikberg Ann-Louise³,Norberg Anna³,Month Stacy⁴,Sandström Herbert⁵,Wahlin Anders¹,Mishima Masanori²,Golovleva Irina³

Affiliation:

1. Department of Radiation Sciences, Umeå University, Umeå, Sweden;

2. Mechanochemical Cell Biology, Division of Biomedical Cell Biology, Warwick Medical School, University of Warwick, Coventry, United Kingdom;

3. Department of Medical Biosciences/Medical and Clinical Genetics, Umeå University, Umeå, Sweden;

4. Department of Pediatric Hematology-Oncology, Kaiser-Permanente, Oakland, CA; and

5. Department of Public Health and Clinical Medicine, Family Medicine, Umeå University, Umeå, Sweden

Abstract

Key Points KIF23/MKLP1 mutation found in the CDA III patients causes cytokinesis failure.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/121/23/4791/1366621/4791.pdf

Reference31 articles.

1. Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts.;Heimpel;Helv Med Acta,1968

2. Congenital dyserythropoietic anemia [in German].;Heimpel;Arch Klin Med,1968

3. Advances in the understanding of the congenital dyserythropoietic anaemias.;Wickramasinghe;Br J Haematol,2005

4. Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III.;Sandström;Eur J Haematol,1994

5. Familial erythroid multinuclearity.;Wolff;Blood,1951

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