Homozygous calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency

Summary

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Authors: Alexandre P. A. Theocharides, Pontus Lundberg, Asvin K. K. Lakkaraju, Veronika Lysenko, Renier Myburgh, Adriano Aguzzi, Radek C. Skoda, Markus G. Manz

Journal title: Blood

Journal number: 127/25

Journal publisher: American Society of Hematology

Published year: 2016

Published pages: 3253-3259

DOI identifier: 10.1182/blood-2016-02-696310

ISSN: 0006-4971