Genotype/phenotype association in von Willebrand disease: Is the glass half full or empty?

Journal of Thrombosis and Haemostasis

Volumn 7, Issue SUPPL. 1, 2009, Pages 65-70

  Lillicrap, David ^a  

^a QUEEN S UNIVERSITY   (Canada)

Author keywords

Genotype; Phenotype; Von Willebrand disease; Von Willebrand factor

Indexed keywords

ALPHA2 INTEGRIN; BLOOD CLOTTING FACTOR 8; GLYCOPROTEIN IB ALPHA; VON WILLEBRAND FACTOR; VON WILLEBRAND FACTOR CLEAVING PROTEINASE;

AMINO ACID SUBSTITUTION; CARBOXY TERMINAL SEQUENCE; DISEASE CLASSIFICATION; GENE DELETION; GENE DISRUPTION; GENE FUNCTION; GENE INTERACTION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOMIC INSTABILITY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MISSENSE MUTATION; MOLECULAR CLONING; MOLECULAR GENETICS; PATHOGENESIS; PHENOTYPIC VARIATION; PRIORITY JOURNAL; QUANTITATIVE TRAIT; REVIEW; THROMBOCYTE ADHESION; THROMBOCYTOPENIA; VON WILLEBRAND DISEASE;

GENETIC VARIATION; HUMANS; PHENOTYPE; VON WILLEBRAND DISEASES; VON WILLEBRAND FACTOR;

EID: 67849118814     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2009.03367.x     Document Type: Review

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