Von Willebrand disease-Phenotype versus genotype: Deficiency versus disease

Thrombosis Research

Volumn 120, Issue SUPPL. 1, 2007, Pages

  Lillicrap, David ^a  

^a QUEEN S UNIVERSITY   (Canada)

Author keywords

Classification of disease; Genetics; Molecular pathology; Mutations; Von Willebrand disease; Von Willebrand factor; VWD; VWF

Indexed keywords

BLOOD CLOTTING FACTOR 8; GLYCOPROTEIN IB; VON WILLEBRAND FACTOR;

ARTICLE; BINDING AFFINITY; CORRELATION ANALYSIS; DIAGNOSTIC TEST; DISEASE CLASSIFICATION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC TRANSCRIPTION; GENOTYPE; HETEROZYGOSITY; HUMAN; INHERITANCE; MISSENSE MUTATION; MOLECULAR WEIGHT; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; QUALITATIVE ANALYSIS; QUANTITATIVE ANALYSIS; RNA SPLICING; THROMBOCYTE ADHESION; VON WILLEBRAND DISEASE;

GENOTYPE; HUMANS; PHENOTYPE; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 34249864402     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.thromres.2007.03.014     Document Type: Article

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