论文信息 - 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 - 字舞流文

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

M. Matsumoto | T. Shigekiyo | K. Udaka | E. Sekimoto | H. Shibata | S. Ozaki | Yukio Higuchi