Silvia Vettore, Raffaella Scandellari, Stefano Moro, Anna Maria Lombardi, Margherita Scapin, Maria Luigia Randi, and Fabrizio Fabris. 2008. “Novel Point Mutation in a Leucine-Rich Repeat of the GPIbα Chain of the Platelet Von Willebrand Factor Receptor, GPIb/IX/V, Resulting in an Inherited Dominant Form of Bernard-Soulier Syndrome Affecting Two Unrelated Families: The N41H Variant”. Haematologica 93 (11). Pavia, Italy, 1743-47. https://doi.org/10.3324/haematol.12830.