Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases

Saved in:

Bibliographic Details
Main Authors:	Fasan, Annette, Haferlach, Claudia, Kohlmann, Alexander, Dicker, Frank, Eder, Christiane, Kern, Wolfgang, Haferlach, Torsten, Schnittger, Susanne
Format:	Artigo
Language:	Inglês
Published:	Ferrata Storti Foundation 2014
Subjects:	Letters to the Editor
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC3912979/ https://ncbi.nlm.nih.gov/pubmed/24497565 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2013.099754
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items