Absence of JAK2-V617F in paroxysmal nocturnal haemoglobinuria-associated thrombosis

Thrombosis and Haemostasis

Volumn 102, Issue 1, 2009, Pages 180-182

  Fouassier, Marc ^a   Girodon, François ^b   Cleyrat, Cédric ^a   Robillard, Nelly ^a   Garand, Richard ^a   Hermouet, Sylvie ^a  

^a NANTES UNIVERSITY HOSPITAL   (France)

^b DIJON UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

UROKINASE RECEPTOR;

ADOLESCENT; ADULT; AGED; ALLELE; BONE MARROW HYPOPLASIA; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; GENE; GENE MUTATION; GRANULOCYTE; HEMATOPOIETIC STEM CELL; HUMAN; HUMAN CELL; INTRAVASCULAR HEMOLYSIS; JAK2 V617F GENE; LETTER; MALE; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PRESCHOOL CHILD; PRIORITY JOURNAL; PRV 1 GENE; THROMBOSIS;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; BUDD-CHIARI SYNDROME; CHILD, PRESCHOOL; FEMALE; HEMOGLOBINURIA, PAROXYSMAL; HUMANS; JANUS KINASE 2; MALE; POINT MUTATION; VENOUS THROMBOSIS; YOUNG ADULT;

EID: 67749132552     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH09-03-0140     Document Type: Letter

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