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Article

Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population.

Neuroscience letters - 15 May 2009

Corominas Roser, Ribasés Marta, Cuenca-León Ester, Narberhaus Bernat, Serra Selma A, del Toro Mireia, Roig Manuel, Fernández-Fernández José M, Macaya Alfons, Cormand Bru

Abstract excerpt

Migraine is a common neurological disorder with a complex inheritance pattern. Mutations in genes encoding proteins that are involved in ion transport across the neuronal membrane have been linked to rare monogenic variants of migraine. These or other related genes and proteins are also candidates to be involved in the inherited predisposition to the more common forms of migraine without aura (MO) or migraine...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19368856
DOI: 10.1016/j.neulet.2009.03.011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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