Screening for c-mpl mutations in patients with congenital amegakaryocytic thrombocytopenia identifies a polymorphism-Reference-Cited by-同舟云学术

Screening for c-mpl mutations in patients with congenital amegakaryocytic thrombocytopenia identifies a polymorphism

Published:2001-06-01 Issue:11 Volume:97 Page:3675-3676
ISSN:1528-0020
Container-title:Blood
language:en
Short-container-title:

Author:

van den Oudenrijn Sonja¹,de Haas Masja¹,Kr. von dem Borne Albert E. G.¹

Affiliation:

1. Correspondence: Albert E.G.Kr. von dem Borne, Department of Hematology, Academic Medical Centre, Meibergdreef 9, Amsterdam, 1105 AZ, The Netherlands

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/97/11/3675/1674076/h8110103668e.pdf

Reference7 articles.

1. Defective response to thrombopoietin and impaired expression of c-mpl mRNA of bone marrow cells in congenital amegakaryocytic thrombocytopenia.;Muraoka;Br J Haematol.,1997

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

3. Acquired amegakaryocytic thrombocytopaenia in a child.;Scarlett;J Paediatr Child Health.,1992

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

5. Identification of mutations in the c-mpl gene in congenital amegakaryocytic thrombocytopenia.;Ihara;Proc Natl Acad Sci U S A.,1999

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