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Article

SERPING1 and F12 combined variants in a hereditary angioedema family.

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology - 1 Oct 2018

Charignon Delphine, Ponard Denise, de Gennes Christian, Drouet Christian, Ghannam Arije

Abstract excerpt

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Topics

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Share to Angioedemas, Hereditary
Share to Bradykinin
Share to Capillary Permeability
Share to Complement C1 Inhibitor Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor XII

Share to Gene Frequency

Share to Glycosylation

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Source

Identifiers

PMID: 29885370
DOI: 10.1016/j.anai.2018.05.031

Genes

SERPING1

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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SERPING1 and F12 combined variants in a hereditary angioedema family.PMID 29885370Read ↗

Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema.Semantic proximity Read ↗

An update on the genetics and pathogenesis of hereditary angioedemaSemantic proximity Read ↗

The Genetics of Hereditary Angioedema: A ReviewSemantic proximity Read ↗

Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene.Semantic proximity Read ↗

Mutation update of SERPING1 related to hereditary angioedema in the Chinese population.Semantic proximity Read ↗

Gene symbol: SERPING1. Disease: Angioneurotic oedema.Semantic proximity Read ↗

Type II hereditary angioedema with an apparently de novo SERPING1 mutation in China: A case report and family screening.Semantic proximity Read ↗

The Expanding Spectrum of Mutations in Hereditary Angioedema.Semantic proximity Read ↗

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

Novel Heterozygous variant of the SERPING1 gene associated with hereditary angioedema in an Italian family based in AustraliaSemantic 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 ↗

A Japanese patient with hereditary angioedema caused by deep intron variation in the SERPING1 gene.Semantic proximity Read ↗

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