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Correspondence
JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia
- Correspondence to Professor Achille Pich, Department of Biomedical Sciences and Human Oncology, Section of Pathology, University of Turin, Via Santena 7, I-10126 Torino, Italy; achille.pich{at}unito.it
Citation
JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia
Publication history
- First published June 20, 2012.
Online issue publication
April 18, 2016
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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.