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Article

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

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology - 1 Nov 2016

Piñero-Saavedra Macarena, González-Quevedo Teresa, Saenz de San Pedro Blanca, Alcaraz Cristina, Bobadilla-González Pedro, Fernández-Vieira Lourdes, Hinojosa Belén, García-Lozano Raúl

Abstract excerpt

BACKGROUND: Information on F12 mutation hereditary angioedema (HAE) is still limited, but Spain is now recognized as having one of the highest concentrations of cases in Western Europe. OBJECTIVE: To describe unique features of HAE in Spanish carriers of the F12 mutation and investigate a potential role for angiotensin-converting enzyme (ACE) and aminopeptidase-P polymorphisms in disease expression. METHODS: This...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Anti-Inflammatory Agents, Non-Steroidal

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Source

Identifiers

PMID: 27788882
DOI: 10.1016/j.anai.2016.09.001

Genes

ACE
XPNPEP2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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