The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2005.05858.x/fullpdf
Reference6 articles.
1. Clinical implications of the JAK2 V617F mutation in essential thrombocythemia
2. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
3. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
4. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
5. A Gain-of-Function Mutation ofJAK2in Myeloproliferative Disorders
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