Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients
This study is a positive contribution towards expanding knowledge about genetic variants in patients with congenital fibrinogen disorders.
Authors
- Angelika Bátorová (ORCID: https://orcid.org/0000-0003-0567-4250)
- Róbert Petrovič (ORCID: https://orcid.org/0000-0002-6789-8447)
- Denisa Jankovičová
- Ján Chandoga
- Pavol Ďurina (ORCID: https://orcid.org/0000-0001-5099-6895)
- Anna Kyselova (ORCID: https://orcid.org/0000-0002-7228-3594)
- Tatiana Prigancová
- Miriama Juhosova
- Silvia Dallemule
- Dominika Jaraskova
- Daniel Böhmer
- Alzbeta Vavrova
Institutions
- University Hospital Bratislava (SK)
- Comenius University Bratislava (SK)
Publication Details
- Journal
- Biomedical Papers
- Published
- 2024-08-16
- DOI
- https://doi.org/10.5507/bp.2024.025
- Primary Topic
- Blood properties and coagulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00