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Platelet dysfunction in platelet-type von Willebrand disease due to the constitutive triggering of the Lyn-PECAM1 inhibitory pathway
Platelet-type von Willebrand disease (PT-VWD) is an inherited platelet disorder. It is characterized by macrothrombocytopenia and mucocutaneous bleeding, of variable severity, due to gain-of-function variants of GP1BA conferring to glycoprotein Ibα (GPIbα) enhanced affinity for von Willebrand factor...
Autores principales: | Bury, Loredana, Falcinelli, Emanuela, Mezzasoma, Anna Maria, Guglielmini, Giuseppe, Momi, Stefania, Gresele, Paolo |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244828/ https://www.ncbi.nlm.nih.gov/pubmed/34407603 http://dx.doi.org/10.3324/haematol.2021.278776 |
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