C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies

INTERNATIONAL JOURNAL OF HEMATOLOGY

Kozubik, KS; Radova, L; Pesova, M; Reblova, K; Trizuljak, J; Plevova, K; Fiamoli, V; Gumulec, J; Urbankova, H; Szotkowski, T; Mayer, J; Pospisilova, S; Doubek, M, 2018: C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies. INTERNATIONAL JOURNAL OF HEMATOLOGY 108(6), p. 652 - 657, doi: 10.1007/s12185-018-2514-3

Research Groups:

• Medical Genomics - Šárka Pospíšilová
• Molecular Oncology - Solid Cancer - Ondřej Slabý
• Behavioural and Social Neuroscience - Milan Brázdil

CEITEC authors:

• Kateřina Staňo Kozubík, Ph.D.
• Lenka Radová, Ph.D.
• Kamila Réblová, Ph.D.
• Prof. Jiří Mayer
• Prof. Michael Doubek, Ph.D.
• Jakub Trizuljak
• Karla Plevová, Ph.D.
• Prof. Šárka Pospíšilová, Ph.D.