A novel C1 inhibitor gene mutation in a family with hereditary angioedema: Use of genetic analysis to facilitate early diagnosis-MedSci.cn

A novel C1 inhibitor gene mutation in a family with hereditary angioedema: Use of genetic analysis to facilitate early diagnosis

Yokoyama, K; Horiuchi, T; Hashimura, C; Yoshida, A

Yokoyama, K (corresponding author), Japanese Red Cross Wakayama Med Ctr, Dept Pediat, Komatsubara 4-20, Wakayama, Wakayama 6408558, Japan.