Nina Borràs
5PUBLICATIONS
4CO-AUTHORS
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Publications (5)
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|Mar 25, 2026
Co-inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction.Perla Bandini, Nina Borràs, Laura Martin-Fernandez
|Jun 27, 2025
Integrating Next-Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real-World Data From Spanish Patients.Nina Borràs, Natàlia Comes, Lorena Ramírez
|Sep 11, 2023
First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.Perla Bandini, Nina Borràs, Eugenia Fernandez Mellid
|Oct 28, 2021
Molecular study of a large cohort of 109 haemophilia patients from Cuba using a gene panel with next generation sequencing-based technology.Nina Borràs, Dunia Castillo-González, Natalia Comes
|Sep 08, 2021
Type 2N VWD: Conclusions from the Spanish PCM-EVW-ES project.Almudena Pérez-Rodríguez, Javier Batlle, Joana Costa Pinto
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