Advances in understanding the pathogenesis of familial myeloproliferative neoplasms
Author:
Affiliation:
1. Department of Haematology Oncology; Fondazione IRCCS Policlinico S. Matteo; Pavia Italy
2. Department of Molecular Medicine; University of Pavia; Pavia Italy
Funder
Associazione Italiana per la Ricerca sul Cancro
AIRC-Gruppo Italiano Malattie Mieloproliferative (AGIMM)
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14713/fullpdf
Reference84 articles.
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2. Endemic polycythemia in Russia: mutation in the VHL gene;Ang;Blood Cells, Molecules, & Diseases,2002
3. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia;Arber;Blood,2016
4. c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia;Ballmaier;Blood,2001
5. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders;Baxter;Lancet,2005
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