Concomitant constitutive LNK and NFE2 mutation with loss of sumoylation in a case of hereditary thrombocythemia

• Lukas Clemens Böckelmann,
• Titiksha Basu,
• Albert Gründer,
• Wei Wang,
• Jan Breucker,
• Sandra Kaiser,
• Andrea Pichler,
• Heike Luise Pahl

Affiliations

Lukas Clemens Böckelmann

Department of Hematology and Oncology, University Medical Center Freiburg, Germany;

Titiksha Basu

Department of Hematology and Oncology, University Medical Center Freiburg, Germany;

Albert Gründer

Department of Hematology and Oncology, University Medical Center Freiburg, Germany;

Wei Wang

Department of Hematology and Oncology, University Medical Center Freiburg, Germany;

Jan Breucker

Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany

Sandra Kaiser

Department of Hematology and Oncology, University Medical Center Freiburg, Germany;

Andrea Pichler

Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany

Heike Luise Pahl

Department of Hematology and Oncology, University Medical Center Freiburg, Germany;