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Identification of a novel candidate splice site mutation (0874 + 1G > A) in a type 3 von Willebrand disease patient.

Thrombosis and haemostasis - 1 Aug 2007

Gadisseur Alain P, Vrelust Inge, Vangenechten Inge, Schneppenheim Reinhard, Van der Planken Marc

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PMID: 17721632

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Identification of a novel candidate splice site mutation (0874 + 1G > A) in a type 3 von Willebrand disease patient.PMID 17721632Read ↗

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An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease.Semantic proximity Read ↗

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Two novel mutations identified in a type 3 von Willebrand disease patient.Semantic proximity Read ↗

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