CO35 | Bleeding phenotype characterization in patients with congenital bleeding disorders: a multigenic approach using next generation sequencing to identify coagulation-modulating variants
Background and Aims: Congenital bleeding disorders, including hemophilia A (HA), hemophilia B (HB), and rare bleeding disorders (RBDs), often display variable clinical phenotypes not fully explained by a single pathogenic variant. Additional genetic variants modulating the coagulation cascade may i...
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| Format: | Article |
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| Language: | English |
| Published: |
PAGEPress Publications
2025-07-01
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| Series: | Bleeding, Thrombosis and Vascular Biology |
| Subjects: | |
| Online Access: | https://www.btvb.org/btvb/article/view/242 |
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