2Janson M, Larsson C, Werelius B, et al. Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus. Proc Natl Acad Sci U S A, 1991, 88:10609-10613.
3Han ED, MacFarlane RC, Mulligan AN, et al. Increased vascular permeability in C1 inhibitor-deficient mice mediated by the bradykinin type 2 receptor. J Clin Invest, 2002, 109:1057-1063.
4Farkas H, Harmat G, Kaposi PN, et al. Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedema. Eur J Gastroenterol Hepatol, 2001, 13:1225-1230.
5Donaldson VH,Evans RR.A biochemical abnormality in hereditary angioneurotic edema:absence of serum inhibitor of C'1-es-terase.Am J Med,1963,35:37-44.
6Agostoni A,Cicardi M.Hereditary and acquired C1-inhibitor deficiency:biological and clinical characteristics in 235 patients.Medicine (Baltimore),1992,71:206-215.
8Janson M,Larsson C,Werelius B,et al.Detailed physical map of human chromosomal region 11q12-13shows high meiotic recombination rate around the MEN1 locus.Proc Natl Acad Sci USA,1991,88:10609-10613.
9Donaldson VH,Rosen FS,Bing DH.Role of the second component of complement (C2) and plasmin in kinin release in hereditary angioneurotic edema (H.A.N.E.) plasma.Trans Assoc Am Physicians,1977,90:174-183.
10Fields T,Ghebrehiwet B,Kaplan AP.Kinin formation in hereditary angioedema plasma:evidence against kinin derivation from C2 and in support of "spontaneous" formation of bradykinin.J Allergy Clin Immunol,1983,72:54-60.