2018年の業績を追加しました。

Yaginuma A, Itoh M, Akasaka E, Nakano H, Sawamura D, Nakagawa H, Asahina A.
Novel mutation c.263A>G in the ACVRL1 gene in a Japanese patient with hereditary hemorrhagic telangiectasia 2.
J Dermatol 2018, in press.