Associated Papers
The Co-Occurrence of Low-Frequency Pathogenic Variants in TBXA2R Exacerbating the Hemorrhagic Symptoms in Siblings with Hemophilia B.
Shimomura M et al.
Seminars in Thrombosis and Hemostasis, 2026
Molecular Pathogenesis of Inherited Platelet Dysfunction.
Rodríguez-Alén A et al.
Biomolecules, 2025
Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease.
Stockley J et al.
Plos One, 2015
How should we test for nonsevere heritable platelet function disorders?
Norman JE et al.
International Journal of Laboratory Hematology, 2014
A novel thromboxane A2 receptor N42S variant results in reduced surface expression and platelet dysfunction.
Nisar SP et al.
Thrombosis and Haemostasis, 2014
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.
Mumford AD et al.
Journal of Thrombosis and Haemostasis : Jth, 2013
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