Recombinant expression of mutations causing von Willebrand disease type Normandy: Characterization of a combined defect of factor VIII binding and multimerization

Thrombosis and Haemostasis

Volumn 92, Issue 1, 2004, Pages 36-41

  Schneppenheim, Reinhard ^a   Lenk, Harald ^b   Obser, Tobias ^a   Oldenburg, Johannes ^c   Oyen, Florian ^a   Schneppenheim, Sonja ^a   Schwaab, Rainer ^d   Will, Kerstin ^e   Budde, Ulrich ^e  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b UNIVERSITY HOSPITAL LEIPZIG   (Germany)

^c GOETHE UNIVERSITY   (Germany)

^d UNIVERSITY OF BONN   (Germany)

^e Labor Prof Arndt and Partner   (Germany)

Author keywords

Multimer structure; Von Willebrand disease type 2N; Von Willebrand factor

Indexed keywords

ADENINE; BLOOD CLOTTING FACTOR 8; CYSTEINE; GUANINE; TYROSINE; VON WILLEBRAND FACTOR;

ADULT; ARTICLE; BINDING SITE; CASE REPORT; CORRELATION ANALYSIS; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; FEMALE; GENE EXPRESSION; GENE MUTATION; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC SCREENING; HEMOPHILIA A; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; LABORATORY TEST; MALE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; QUANTITATIVE ANALYSIS; RECESSIVE INHERITANCE; VON WILLEBRAND DISEASE;

EID: 3543041260     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/th04-02-0084     Document Type: Article

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