A founder mutation in the MPL gene causes congenital amegakaryocytic thrombocytopenia (CAMT) in the Ashkenazi Jewish population-Reference-Cited by-同舟云学术

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A founder mutation in the MPL gene causes congenital amegakaryocytic thrombocytopenia (CAMT) in the Ashkenazi Jewish population

Published:2011-06 Issue:1 Volume:47 Page:79-83
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Jalas Chaim,Anderson Sylvia L.,Laufer Tova,Martimucci Kristina,Bulanov Alex,Xie Xie,Ekstein Josef,Rubin Berish Y.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference33 articles.

1. Congenital amegakaryocytic thrombocytopenia: an intrinsic hematopoietic stem cell defect;Freedman;Am. J. Pediatr. Hematol. Oncol.,1990

2. Amegakaryocytic thrombocytopenia;Alter,1993

3. Thrombopoietin is essential for the maintenance of normal hematopoiesis in humans: development of aplastic anemia in patients with congenital amegakaryocytic thrombocytopenia;Ballmaier;Ann. N. Y. Acad. Sci.,2003

4. Mutations in the thrombopoietin receptor, Mpl, in children with congenital amegakaryocytic thrombocytopenia;van den Oudenrijn;Br. J. Haematol.,2000

5. Congenital amegakaryocytic thrombocytopenia: a retrospective clinical analysis of 20 patients;King;Br. J. Haematol.,2005

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