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Article

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine.

Archives of neurology - 1 Jun 2004

Jen Joanna C, Kim Gilbert W, Dudding Kristen A, Baloh Robert W

Abstract excerpt

BACKGROUND: Mutations in CACNA1A, encoding a neuronal calcium channel subunit, and ATP1A2, encoding a catalytic subunit of a sodium-potassium-ATPase, have been found in some families with dominantly inherited hemiplegic migraine. OBJECTIVE: To determine the prevalence of mutations in these genes in individuals with different migraine syndromes. DESIGN: Prospective screening study. SETTING: University outpatient...

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Identifiers

PMID: 15210532
DOI: 10.1001/archneur.61.6.926

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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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The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura.Semantic proximity Read ↗

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