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Article

[From gene to disease; from CACNA1A to migraine].

Nederlands tijdschrift voor geneeskunde - 10 Feb 2001

Kors E E, Haan J, Frants R R, Ferrari M D

Abstract excerpt

Familial hemiplegic migraine (FHM) is a rare autosomal dominant subtype of migraine with aura. FHM is associated in half the families with mutations in the CACNA1A gene on chromosome 19P13, encoding the alpha-1A subunit of brain-specific P/Q-type calcium channels. P/Q-type calcium channels are im...

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PMID: 11236374

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-11236374-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

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

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[From gene to disease; from CACNA1A to migraine].PMID 11236374Read ↗

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The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.Semantic proximity Read ↗

[Role of P/Q calcium channel in familial hemiplegic migraine].Semantic proximity Read ↗

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