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

M Despotović

M Despotović

University of Rijeka, Faculty of MedicineRijeka, Croatia
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Despotović, M
, 
N Pereza

N Pereza

Department of Medical Biology and Genetics, University of Rijeka, Faculty of MedicineRijeka, Croatia
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Pereza, N
, 
B Peterlin

B Peterlin

Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
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Peterlin, B
, 
S Ostojić

S Ostojić

Department of Medical Biology and Genetics, University of Rijeka, Faculty of MedicineRijeka, Croatia
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Ostojić, S
, 
B Golob

B Golob

Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
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Golob, B
, 
A Maver

A Maver

Clinical Institute for Genomic Medicine, University Medical Centre LjubljanaLjubljana, Slovenia
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Maver, A
 and 
J Roganović

J Roganović

Department of Pediatrics, Clinical Hospital Center RijekaRijeka, Croatia
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Roganović, J
  
Mar 01, 2023
A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia's Cover Image
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Article Category: Case Report
Published Online: Mar 01, 2023
Page range: 85 - 88
DOI: https://doi.org/10.2478/bjmg-2022-0009
Keywords
© 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.
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Basic Medical Science, Basic Medical Science, other
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