What we have learned from inherited platelet disorders

Pediatric Blood and Cancer

Volumn 60, Issue SUPPL.1, 2013, Pages

  Israels, Sara J ^a   Rand, Margaret L ^b  

^a UNIVERSITY OF MANITOBA   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Genotype phenotype associations; Platelet disorders; Platelet function; Review

Indexed keywords

CYTOSKELETON PROTEIN; MEMBRANE PROTEIN; MYOSIN HEAVY CHAIN; THROMBOXANE A2; VON WILLEBRAND FACTOR;

ATHEROSCLEROTIC PLAQUE; BERNARD SOULIER DISEASE; BRAIN ISCHEMIA; CANCER GROWTH; CYTOSKELETON; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; GLANZMANN DISEASE; GRAY PLATELET SYNDROME; GROWTH; HEMOSTASIS; HUMAN; IMMUNE RESPONSE; LUNG FIBROSIS; MAY HEGGLIN ANOMALY; NONHUMAN; OCULAR ALBINISM; PRIORITY JOURNAL; RECEPTOR DENSITY; REVIEW; SCOTT SYNDROME; SIGNAL TRANSDUCTION; THROMBOCYTE ACTIVATION; THROMBOCYTE ADHESION; THROMBOCYTE AGGLUTINATION; THROMBOCYTE AGGREGATION; THROMBOCYTE COUNT; THROMBOCYTE DISORDER; THROMBOCYTE FUNCTION; THROMBOCYTE MEMBRANE; THROMBOCYTE SHAPE; THROMBOCYTOPENIA; THROMBOCYTOPOIESIS; THROMBOEMBOLISM; THROMBOSIS;

BLOOD PLATELET DISORDERS; BLOOD PLATELETS; GENETIC ASSOCIATION STUDIES; GENOME-WIDE ASSOCIATION STUDY; HEMORRHAGE; HEMOSTASIS; HUMANS; PHENOTYPE; PLATELET ADHESIVENESS; POLYMORPHISM, GENETIC; THROMBOSIS;

EID: 84869214159     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.24345     Document Type: Review

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