Type 2N von Willebrand disease: rapid genetic diagnosis of G2811A (R854Q), C2696T (R816W), T2701A (H817Q) and G2823T (C858F) – detection of a novel candidate type 2N mutation: C2810T (R854W) - Bowen, DJ; Standen, GR; Mazurier, C (Thromb Haemost, 1998)
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