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CACNA1A gene mutations in familial hemiplegic migraine

โœ Scribed by Arn M.J.M. van den Maagdenberg; Joerg Striessnig; Michel D. Ferrari; Rune R. Frants

Publisher
Springer
Year
2000
Tongue
English
Weight
217 KB
Volume
1
Category
Article
ISSN
1129-2369

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We searched for mutations in the voltagegated 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 a

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Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. The disease is caused by mutations of at least three genes among which two have been identified, CACNA1A and ATP1A2. Very few mutations have been identified so far in ATP1A2. We screened the coding sequence of AT