Factor VII Mie: homozygous asymptomatic type I deficiency caused by an amino acid substitution of His (CAC) for Arg (247) (CGC) in the catalytic domain - Ohiwa, M; Hayashi, T; Wada, H; Minamikawa, K; Shirakawa, S; Suzuki, K (Thromb. Haemost, 1994)