T. Kashiwagi

L1503R is a member of group I mutation and has dominant‐negative effect on secretion of full‐length VWF multimers: an analysis of two patients with type 2A von Willebrand disease

T. Naoe, T. Murate, J. Takamatsu, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

An Sp1 binding site mutation of the PROS1 promoter in a patient with protein S deficiency

T. Naoe, T. Murate, T. Matsushita, 2007, British journal of haematology.

Molecular defects associated with antithrombin deficiency and dilated cardiomyopathy in a Japanese patient.

K. Node, K. Nagata, T. Murate, 2008, Internal medicine.