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Analysis of platelet membrane glycoprotein polymorphisms in Glanzmann thrombasthenia showed the French gypsy mutation in the αIIb gene to be strongly linked to the HPA-1b polymorphism in β3

Archive ouverte | Jacquelin, B. | CCSD

International audience. We have tested the DNA of a large series of Glanzmann thrombasthenia patients for polymorphisms in platelet membrane glycoproteins. To our surprise, we noted a high prevalence of the HPA-1b a...

Kindlin-2 in platelets and in megakaryocytes: a possible role in beta integrin activation

Archive ouverte | Ghalloussi, D. | CCSD

International audience

Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features

Archive ouverte | Saultier, Paul | CCSD

Congenital macrothrombocytopenia is a family of rare diseases, of which a significant fraction remains to be genetically characterized. To analyze cases of unexplained thrombocytopenia, 27 individuals from a patient cohort of the ...

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