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A Novel ATP1A2 Gene Mutation in an Irish Familial Hemiplegic Migraine Kindred

✍ Scribed by Desiree M. Fernandez; Collette K. Hand; Brian J. Sweeney; Nollaig A. Parfrey


Book ID
109100004
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
224 KB
Volume
0
Category
Article
ISSN
0017-8748

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ATP1A2 mutations in 11 families with fam
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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