Mahiru Tokoro

Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing.

F. Hayakawa, T. Matsushita, A. Takagi, 2019, Thrombosis research.

Aberrant X chromosomal rearrangement through multi‐step template switching during sister chromatid formation in a patient with severe hemophilia A

F. Hayakawa, T. Matsushita, A. Takagi, 2020, Molecular genetics & genomic medicine.

Essential role of a carboxyl‐terminal α‐helix motif in the secretion of coagulation factor XI

F. Hayakawa, T. Matsushita, A. Takagi, 2021, Journal of thrombosis and haemostasis : JTH.

F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B.

F. Hayakawa, T. Matsushita, K. Nogami, 2022, Thrombosis research.

Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency.

F. Hayakawa, T. Matsushita, A. Takagi, 2019, Thrombosis research.