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Article

Familial migraine with vertigo: no mutations found in CACNA1A.

American journal of medical genetics - 1 Sept 1998

Kim J S, Yue Q, Jen J C, Nelson S F, Baloh R W

Abstract excerpt

We searched for mutations in the voltage-gated calcium channel gene, CACNA1A, in nine propositi of families with migraine headaches and episodic vertigo inherited in an autosomal dominant pattern. All 47 exons and flanking introns in CACNA1A were subjected to single-strand conformation polymorphism analysis of polymerase chain reaction-amplified genomic DNA. Exons with aberrantly migrating fragments were...

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Source

Identifiers

PMID: 9741473
DOI: 10.1002/(sici)1096-8628(19980901)79:2<148::aid-ajmg11>3.0.co;2-j

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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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Familial migraine with vertigo: no mutations found in CACNA1A.PMID 9741473Read ↗

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De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia.Semantic proximity Read ↗

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Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.Semantic proximity Read ↗

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine.Semantic proximity Read ↗

Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene.Semantic proximity Read ↗

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