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Listar por palabra clave "Single-strand conformation polymorphism: Type 2 vWD"

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Search for Mutations in a Segment of the Exon 28 of the Human Von Willebrand Factor Gene. New Mutations, R1315C and R1341W, Associated with Type 2M and 2B Variants

Casaña, Pilar; Martínez, Francisco; Espinós-Armero, Carmen Ángeles; Haya, Saturnino; Lorenzo, José Ignacio; Aznar, José A. (John Wiley & Sons, 1998-09)

[EN] von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF), A large number of defects ...

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