A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia
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01 mar 2023
INFORMAZIONI SU QUESTO ARTICOLO
Categoria dell'articolo: Case Report
Pubblicato online: 01 mar 2023
Pagine: 85 - 88
DOI: https://doi.org/10.2478/bjmg-2022-0009
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© 2022 Despotović M, Pereza N, Peterlin B, Ostojić S, Golob B, Maver A, Roganović J, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Despotović, M
University of Rijeka, Faculty of MedicineRijeka, Croatia
Pereza, N
Department of Medical Biology and Genetics, University of Rijeka, Faculty of MedicineRijeka, Croatia
Peterlin, B
Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
Ostojić, S
Department of Medical Biology and Genetics, University of Rijeka, Faculty of MedicineRijeka, Croatia
Golob, B
Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
Maver, A
Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
Roganović, J
Department of Pediatrics, Clinical Hospital Center RijekaRijeka, Croatia