Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A,Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM. Increased activity ofcoagulation factor XII (Hageman factor) causes hereditary angioedema type III. AmJ Hum Genet. 2006 Dec;79(6):1098-104.
Dewald G, Bork K. Missense mutations in the coagulation factor XII (Hagemanfactor) gene in hereditary angioedema with normal C1 inhibitor. Biochem BiophysRes Commun. 2006 May 19;343(4):1286-9.
Lombardi AM, Bortoletto E, Scarparo P, Scapin M, Santarossa L, Girolami A.Genetic study in patients with factor XII deficiency: a report of three newmutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in threecompound heterozygotes. Blood Coagul Fibrinolysis. 2008 Oct;19(7):639-43. doi:10.1097/MBC.0b013e32830d8629.
Martin L, Raison-Peyron N, Nöthen MM, Cichon S, Drouet C. Hereditaryangioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene. J Allergy ClinImmunol. 2007 Oct;120(4):975-7.
Renné T, Gailani D. Role of Factor XII in hemostasis and thrombosis: clinical implications. Expert Rev Cardiovasc Ther. 2007 Jul;5(4):733-41. Review.
Schmaier AH. The elusive physiologic role of Factor XII. J Clin Invest. 2008Sep;118(9):3006-9. doi: 10.1172/JCI36617. Review.
Contributor
MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register
: Vivi Li
You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
OK
Confirm
Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?