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A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia

Open Access
|Mar 2023

Authors

M Despotović

despotovicmarta@gmail.com

University of Rijeka, Faculty of Medicine, Rijeka, Croatia

N Pereza

Department of Medical Biology and Genetics, University of Rijeka, Faculty of Medicine, Rijeka, Croatia

B Peterlin

Clinical Institute for Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia

S Ostojić

Department of Medical Biology and Genetics, University of Rijeka, Faculty of Medicine, Rijeka, Croatia

B Golob

Clinical Institute for Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia

A Maver

Clinical Institute for Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia

J Roganović

Department of Pediatrics, Clinical Hospital Center Rijeka, Rijeka, Croatia
Language: English
Page range: 85 - 88
Published on: Mar 1, 2023
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2023 M Despotović, N Pereza, B Peterlin, S Ostojić, B Golob, A Maver, J Roganović, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.