| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3798297 | Medicina Clínica | 2012 | 6 Pages |
Abstract
The presence of V617F mutation is associated with a higher incidence of thrombosis, leukocytosis and splenomegaly. The identification of mutation on the JAK2 gene could help in a better definition of evolution and prognostic stratification of the myeloproliferative disorders.
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Medicine and Dentistry (General)
Authors
Ana Esther Kerguelén Fuentes, Dolores Hernández-Maraver, Luis Lombardia, Miguel Angel Canales Albendea, Ana Rodriguez de la Rúa,