Hereditary angioedema with normal C1 inhibitor function: Consensus of an international expert panel
B.L. Zuraw, K. Bork, and K.E. Binkley Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel Allergy Asthma Proc 33 suppl 1 2012 S145 S156
Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor
G. Dewald, and K. Bork Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor Biochem Biophys Res Commun 343 2006 1286 1289
A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor
K. Bork, K. Wulff, P. Meinke, N. Wagner, J. Hardt, and G. Witzke A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor Clin Immunol 141 2011 31 35
Factor XII Osaka: Abnormal factor XII with partially defective prekallikrein cleavage activity
K. Iijima, Y. Arakawa, and Y. Sugahara Factor XII Osaka: abnormal factor XII with partially defective prekallikrein cleavage activity Thromb Haemost 105 2011 473 478
The novel acceptor splice site mutation 11396(G→A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients
M. Schloesser, S. Hofferbert, U. Bartz, G. Lutze, B. Lämmle, and W. Engel The novel acceptor splice site mutation 11396(G→A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients Hum Mol Genet 4 1995 1235 1237
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome
F. Bu, T. Maga, and N.C. Meyer Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome J Am Soc Nephrol 25 2014 55 64