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Article

Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: A multifactorial disease

10 Jul 2013

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Share to Autoimmune Bullous Skin Diseases
Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23849223
DOI: 10.1016/j.jaci.2013.04.032

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: A multifactorial diseasePMID 23849223Read ↗

A rare mutation in the F12 gene in a patient with ACE inhibitor-induced angioedema.Semantic proximity Read ↗

Hereditary angioedema with F12 mutation: first report of three cases associated with immune disorders.Semantic proximity Read ↗

Idiopathic angioedema with F12 mutation: is it a new entity?Semantic proximity Read ↗

Hereditary angioedema with F12 mutation: Clinical features and enzyme polymorphisms in 9 Southwestern Spanish families.Semantic proximity Read ↗

SERPING1 and F12 combined variants in a hereditary angioedema family.Semantic proximity Read ↗

In Silico Analysis and In-depth Assessment of a Female Patient with a Missense Mutation in the F12 Gene Associated with Hereditary Angioedema Symptoms: A Case StudySemantic proximity Read ↗

Characterization of patients with angioedema without wheals: the importance of F12 gene screening.Semantic proximity Read ↗

A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.Semantic proximity Read ↗

Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.Semantic proximity Read ↗

Novel duplication in the F12 gene in a patient with recurrent angioedema.Semantic proximity Read ↗

Hereditary angioedema with a mutation in the plasminogen gene.Semantic proximity Read ↗

Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor.Semantic proximity Read ↗

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