Identification of a homozygous missense mutation (p.Cys379Gly) in the D1 domain of von Willebrand factor propeptide in a family with type 2A (IIC) von Willebrand disease

Haemophilia, EarlyView.

Source: Haemophilia - September 3, 2018 Category: Hematology Authors: Toshio Shigekiyo , Kengo Udaka , Etsuko Sekimoto , Hironobu Shibata , Shuji Ozaki , Yukio Higuchi , Masanori Matsumoto Source Type: research