Articles

JUNB, DUSP2, SGK1, SOCS1 and CREBBP are frequently mutated in T-cell/histiocyte-rich large B-cell lymphoma

Dr. Senckenberg Institute of Pathology, Goethe University, Frankfurt am Main, Germany
Dr. Senckenberg Institute of Pathology, Goethe University, Frankfurt am Main, Germany
Genecore, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany;Genome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
Genecore, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
Department of Pathology, University Hospitals K.U. Leuven, Belgium
Department of Pathology, Tampere University Hospital and University of Tampere, Finland
Unit of Lymphoid Malignancies, Department of Pathology, Scientific Institute San Raffaele, Milan, Italy
José Carreras Center for Immuno and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg, Saar, Germany;Department of Internal Medicine 2, Hospital of the J. W. Goethe University, Frankfurt am Main, Germany
Department of Pathology and Laboratory Medicine and the Centre for Lymphoid Cancer, British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada
Department of Pathology and Laboratory Medicine and the Centre for Lymphoid Cancer, British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada
Institute of Cell Biology (Cancer Research), Faculty of Medicine, University of Duisburg-Essen, Essen, Germany;Deutsches Konsortium für Translationale Krebsforschung (DKTK), Germany
Dr. Senckenberg Institute of Pathology, Goethe University, Frankfurt am Main, Germany;Reference and Consultant Center for Lymphoma and Lymph Node Diagnostics, Goethe University, Frankfurt am Main, Germany;Frankfurt Institute of Advanced Studies, Frankfurt am Main, Germany
Dr. Senckenberg Institute of Pathology, Goethe University, Frankfurt am Main, Germany;Reference and Consultant Center for Lymphoma and Lymph Node Diagnostics, Goethe University, Frankfurt am Main, Germany
Vol. 104 No. 2 (2019): February, 2019 https://doi.org/10.3324/haematol.2018.203224