Haematologica (Feb 2014)

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

Annette Fasan,
Claudia Haferlach,
Alexander Kohlmann,
Frank Dicker,
Christiane Eder,
Wolfgang Kern,
Torsten Haferlach,
Susanne Schnittger

Affiliations

Annette Fasan: MLL Munich Leukemia Laboratory, Munich, Germany
Claudia Haferlach: MLL Munich Leukemia Laboratory, Munich, Germany
Alexander Kohlmann: MLL Munich Leukemia Laboratory, Munich, Germany
Frank Dicker: MLL Munich Leukemia Laboratory, Munich, Germany
Christiane Eder: MLL Munich Leukemia Laboratory, Munich, Germany
Wolfgang Kern: MLL Munich Leukemia Laboratory, Munich, Germany
Torsten Haferlach: MLL Munich Leukemia Laboratory, Munich, Germany
Susanne Schnittger: MLL Munich Leukemia Laboratory, Munich, Germany

DOI: https://doi.org/10.3324/haematol.2013.099754
Journal volume & issue: Vol. 99, no. 2

Abstract

No abstracts available.

Published in Haematologica

ISSN: 0390-6078 (Print); 1592-8721 (Online)
Publisher: Ferrata Storti Foundation
Country of publisher: Italy
LCC subjects: Medicine: Internal medicine: Specialties of internal medicine: Diseases of the blood and blood-forming organs
Website: http://www.haematologica.org

About the journal