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1. Co-existence of JAK2 V617F and CALR mutations in primary myelofibrosis.

Author

Zamora L, Xicoy B, Cabezón M, Fernandez C, Marcé S, Velez P, Xandri M, Gallardo D, Millá F, Feliu E, and Boqué C

Subjects
Genetic Association Studies, Genetic Predisposition to Disease, Humans, Primary Myelofibrosis diagnosis, Calreticulin genetics, Codon, Janus Kinase 2 genetics, Mutation, Primary Myelofibrosis genetics
Published
2015
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