The investigation of JAK2 mutation in Chinese myeloproliferative diseases-identification of a novel C616Y point mutation in a PV patient
Author:
Publisher
Wiley
Subject
Hematology,Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.2006.00864.x/fullpdf
Reference6 articles.
1. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
2. Management of Polycythemia Vera and Essential Thrombocythemia
3. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
4. A Gain-of-Function Mutation ofJAK2in Myeloproliferative Disorders
5. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
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