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

Kateřina Staňo Kozubík, Lenka Radová, Michaela Pešová, Kamila Réblová, Jakub Trizuljak, Karla Plevová, Veronika Fiamoli, Jaromír Gumulec, Helena Urbánková, Tomáš Szotkowski, Jiří Mayer, Šárka Pospíšilová, Michael Doubek*

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology