A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia
By:
Authors
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
DOI: https://doi.org/10.2478/bjmg-2022-0009 | Journal eISSN: 2199-5761
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
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© 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.