Similarity in joint and mucous bleeding syndromes in type 2N von Willebrand disease and severe hemophilia A coexisting with type 1 von Willebrand disease in two Chinese pedigrees-Reference-Cited by-同舟云学术

Similarity in joint and mucous bleeding syndromes in type 2N von Willebrand disease and severe hemophilia A coexisting with type 1 von Willebrand disease in two Chinese pedigrees

Published:2014-04 Issue:4 Volume:52 Page:181-185
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Qin H.H.,Xing Z.F.,Wang X.F.,Ding Q.L.,Xi X.D.,Wang H.L.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference22 articles.

1. Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study;Eikenboom;J. Thromb. Haemost.,2009

2. Factor VIII–von Willebrand factor binding defects in autosomal recessive von Willebrand disease type Normandy and in mild hemophilia A. New insights into factor VIII–von Willebrand factor interactions;Jacquemin;Acta Haematol.,2009

3. Factor VIII (FVIII) gene mutations in 120 patients with hemophilia A: detection of 26 novel mutations and correlation with FVIII inhibitor development;Repesse;J. Thromb. Haemost.,2007

4. Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations;Jokela;Haemophilia,2013

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