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Volumn 8, Issue 1, 2010, Pages 21-27

Is the absence of JAK2V617F mutation a risk factor for bleeding in essential thrombocythemia? An analysis of 106 patients

Author keywords

Bleeding; Essential thrombocythaemia; JAK2V617F; Myeloproliferative disorders; Thrombosis

Indexed keywords

ADULT; AGED; ARTICLE; BLEEDING; BLOOD CELL COUNT; CARDIOVASCULAR RISK; COHORT ANALYSIS; CONTROLLED STUDY; CORRELATION ANALYSIS; CYTOREDUCTIVE SURGERY; FEMALE; FOLLOW UP; GENE; GENE MUTATION; GENE OVEREXPRESSION; GENETIC ASSOCIATION; HEMATOCRIT; HUMAN; JANUS KINASE 2 V617F GENE; LABORATORY TEST; LEUKOCYTE COUNT; MAJOR CLINICAL STUDY; MALE; PRV1 GENE; RETROSPECTIVE STUDY; RISK FACTOR; STATISTICAL SIGNIFICANCE; THROMBOCYTE COUNT; THROMBOSIS; THROMBOTIC THROMBOCYTOPENIC PURPURA; UNIVARIATE ANALYSIS; WILD TYPE; AMINO ACID SUBSTITUTION; BLOOD; GENETICS; LEUKOCYTE; METABOLISM; MIDDLE AGED; MISSENSE MUTATION; THROMBOCYTHEMIA;

EID: 74549226161     PISSN: 17232007     EISSN: None     Source Type: Journal    
DOI: 10.2450/2009.0004-09     Document Type: Article
Times cited : (17)

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