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A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia
Balkan Journal of Medical Genetics, 25 (2023), 1; 85-88. https://doi.org/10.2478/bjmg-2022-0009

Despotović, Marta; Pereza, Nina; Peterlin, Borut; Ostojić, Saša; Golob, B; Maver, A; Roganović, Jelena

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Despotović, M., Pereza, N., Peterlin, B., Ostojić, S., Golob, B., Maver, A. i Roganović, J. (2023). A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia. Balkan Journal of Medical Genetics, 25. (1), 85-88. doi: 10.2478/bjmg-2022-0009

Despotović, Marta, et al. "A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia." Balkan Journal of Medical Genetics, vol. 25, br. 1, 2023, str. 85-88. https://doi.org/10.2478/bjmg-2022-0009

Despotović, Marta, Nina Pereza, Borut Peterlin, Saša Ostojić, B Golob, A Maver i Jelena Roganović. "A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia." Balkan Journal of Medical Genetics 25, br. 1 (2023): 85-88. https://doi.org/10.2478/bjmg-2022-0009

Despotović, M., et al. (2023) 'A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia', Balkan Journal of Medical Genetics, 25(1), str. 85-88. doi: 10.2478/bjmg-2022-0009

Despotović M, Pereza N, Peterlin B, Ostojić S, Golob B, Maver A, i sur.. A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia. Balkan Journal of Medical Genetics [Internet]. 01.03.2023. [pristupljeno 18.07.2024.];25(1):85-88. doi: 10.2478/bjmg-2022-0009

M. Despotović, et al., "A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia", Balkan Journal of Medical Genetics, vol. 25, br. 1, str. 85-88, Ožujak 2023. [Online]. Dostupno na: https://urn.nsk.hr/urn:nbn:hr:184:600519. [Citirano: 18.07.2024.]