Hereditary angioedema in Greek families caused by novel and recurrent mutations
Authors:
- Matthaios SpeletasMSMatthaios Speletas
- Konstantinos BoukasKBKonstantinos Boukas
- Efimia Papadopoulou-AlatakiEPEfimia Papadopoulou-Alataki
- Elena TsitsamiETElena Tsitsami
- Anastasios E. GermenisAGAnastasios E. Germenis
- 1 November 2009
- journal article
- research article
- Published by Elsevier in Human Immunology
- Vol. 70 (11) , 925-929
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Kallikrein–kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309LysBlood Coagulation & Fibrinolysis, 2009
- Hereditary AngioedemaNew England Journal of Medicine, 2008
- Hereditary Angioedema with Normal C1 Inhibitor: Clinical Symptoms and CourseThe American Journal of Medicine, 2007
- Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type IIIThe American Journal of Human Genetics, 2006
- Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitorBiochemical and Biophysical Research Communications, 2006
- Deficiencies of C1 inhibitorBest Practice & Research Clinical Gastroenterology, 2005
- A Review of the Reported Defects in the Human C1 Esterase Inhibitor Gene Producing Hereditary Angioedema Including Four New MutationsClinical Immunology, 2001
- Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedemaJournal of Allergy and Clinical Immunology, 2000
- Hereditary angioedema with normal C1-inhibitor activity in womenThe Lancet, 2000
- Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements.Proceedings of the National Academy of Sciences, 1990