Haematologica
(Mar 2019)
Clinical implications of subclonal TP53 mutations in acute myeloid leukemia
Katharina T. Prochazka,
Gudrun Pregartner,
Frank G. Rücker,
Ellen Heitzer,
Gabriel Pabst,
Albert Wölfler,
Armin Zebisch,
Andrea Berghold,
Konstanze Döhner,
Heinz Sill
Affiliations
Katharina T. Prochazka
Division of Hematology, Medical University of Graz, Austria
Gudrun Pregartner
Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, Austria
Frank G. Rücker
Department of Internal Medicine III, University Hospital of Ulm, Germany
Ellen Heitzer
Institute of Human Genetics, Medical University of Graz, Austria
Gabriel Pabst
Division of Hematology, Medical University of Graz, Austria
Albert Wölfler
Division of Hematology, Medical University of Graz, Austria
Armin Zebisch
Division of Hematology, Medical University of Graz, Austria
Andrea Berghold
Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, Austria
Konstanze Döhner
Department of Internal Medicine III, University Hospital of Ulm, Germany
Heinz Sill
Division of Hematology, Medical University of Graz, Austria
DOI
https://doi.org/10.3324/haematol.2018.205013
Journal volume & issue
Vol. 104,
no. 3
Abstract
Read online
The role of subclonal TP53 mutations, defined by a variant allele frequency of 40%, 20%-40% and 40%, 19 had variant allele frequencies between 20%-40% and 18 had frequencies
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
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