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Analysis of phenotype and outcome in essential thrombocythemia with CALR or JAK2 mutations
The JAK2 V617F mutation, the thrombopoietin receptor MPL W515K/L mutation and calreticulin (CALR) mutations are mutually exclusive in essential thrombocythemia and support a novel molecular categorization of essential thrombocythemia. CALR mutations account for approximately 30% of cases of essentia...
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| Veröffentlicht in: | Haematologica |
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| Hauptverfasser: | , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Ferrata Storti Foundation
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4486223/ https://ncbi.nlm.nih.gov/pubmed/25934766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2014.118299 |
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