A family having type 2B von Willebrand disease with a novel VWF p.R1308S mutation: Detection of characteristic platelet aggregates on peripheral blood smears as the key aspect of diagnosis-Reference-Cited by-同舟云学术

A family having type 2B von Willebrand disease with a novel VWF p.R1308S mutation: Detection of characteristic platelet aggregates on peripheral blood smears as the key aspect of diagnosis

Published:2015-10 Issue:4 Volume:136 Page:813-817
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Hatta Kyoko,Kunishima Shinji,Suganuma Hiroki,Tanaka Noboru,Ohkawa Natsuki,Shimizu Toshiaki

Publisher

Elsevier BV

Subject

Hematology

Reference33 articles.

1. Inherited thrombocytopenias: the evolving spectrum;Balduini;Hamostaseologie,2012

2. Congenital macrothrombocytopenias;Kunishima;Blood Rev.,2006

3. Misdiagnosis of chronic thrombocytopenia in childhood;Bader-Meunier;J. Pediatr. Hematol. Oncol.,2003

4. ACTN1 mutations cause congenital macrothrombocytopenia;Kunishima;Am. J. Hum. Genet.,2013

5. von Willebrand factor and von Willebrand disease;Ruggeri;Blood,1987

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