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Spectrum of ASXL1 mutations in primary myelofibrosis: prognostic impact of the ASXL1 p.G646Wfs*12 mutation.

Academic Article
Publication Date:
2019
abstract:
Data reported herein suggest that care should be taken to accurately detect and report the ASXL1G646Wfs*12 variant in patients with PMF because of its strong adverse impact on OS and LFS.
Iris type:
1.1 Articolo in rivista
Keywords:
asxl1, myelofibrosis
List of contributors:
Rotunno, G; Mannarelli, C; Brogi, G; Pacilli, A; Gesullo, F; Mannelli, F; Fiaccabrino, S; Sordi, B; Paoli, C; Marone, I; Rumi, E; Manfredini, R; Barosi, G; Cazzola, M; Vannucchi, Am; Guglielmelli, P.
Authors of the University:
RUMI ELISA
Handle:
https://iris.unipv.it/handle/11571/1321870
Published in:
BLOOD
Journal
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URL

https://www.ncbi.nlm.nih.gov/pubmed/31076447
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