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Landolfi, Raffaele

One or more keywords matched the following items that are connected to Landolfi, Raffaele

Item Type	Name
Concept	Receptor, PAR-1
Academic Article	Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype.
Academic Article	Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome.

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Receptor PAR 2

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