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

Blood Cells, Molecules, and Diseases

Volumn 52, Issue 4, 2014, Pages 181-185

  Qin, H H ^a,b   Xing, Z F ^a   Wang, X F ^b   Ding, Q L ^b   Xi, X D ^a   Wang, H L ^a  

^a Shanghai Institute of Hematology   (China)

^b SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

FVIII; HA; Molecular pathogenesis; Type 2N; VWD; VWF

Indexed keywords

BLOOD CLOTTING FACTOR 8; VON WILLEBRAND FACTOR;

ADULT; ARTICLE; BLOOD CLOTTING FACTOR 8 GENE; CASE REPORT; CELL STRAIN HEK293; CHILD; CHINESE; CLINICAL FEATURE; COMORBIDITY; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HEMARTHROSIS; HEMOPHILIA A; HUMAN; MALE; MOLECULAR PATHOLOGY; MUCOSAL BLEEDING; MUTATIONAL ANALYSIS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; VON WILLEBRAND DISEASE; VON WILLEBRAND DISEASE TYPE 2N; VON WILLEBRAND FACTOR GENE;

FVIII; HA; MOLECULAR PATHOGENESIS; TYPE 2N; VWD; VWF;

ADULT; BLOOD COAGULATION TESTS; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FACTOR VIII; FEMALE; GENOTYPE; HEMARTHROSIS; HEMOPHILIA A; HEMORRHAGE; HUMANS; MALE; MUCOUS MEMBRANE; MUTATION; PHENOTYPE; PROTEIN BINDING; VON WILLEBRAND DISEASE, TYPE 1; VON WILLEBRAND DISEASE, TYPE 2; VON WILLEBRAND FACTOR;

EID: 84895539236     PISSN: 10799796     EISSN: 10960961     Source Type: Journal    
DOI: 10.1016/j.bcmd.2013.11.005     Document Type: Article

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