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Article

The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility.

Neuroscience letters - 27 Mar 2009

D'Onofrio Mara, Ambrosini Anna, Di Mambro Alessandra, Arisi Ivan, Santorelli Filippo M, Grieco Gaetano S, Nicoletti Ferdinando, Nappi Giuseppe, Pierelli Francesco, Schoenen Jean, Buzzi Maria Gabriella

Abstract excerpt

Migraine is a common disorder with a significant genetic component. Mutations in the CACNA1A gene are found in hemiplegic migraine (HM). Basilar-type (BM), another subtype of migraine with aura, differs from HM only by the absence of motor deficits. BM and HM may thus share common genetic feature...

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Source

Identifiers

PMID: 19429006
DOI: 10.1016/j.neulet.2009.01.081

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19429006-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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