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Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation

✍ Scribed by A Lebas; L Guyant-Maréchal; D Hannequin; F Riant; E Tournier-Lasserve; D Parain

Book ID
111092869
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
214 KB
Volume
28
Category
Article
ISSN
0333-1024

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ATP1A2 mutations in 11 families with fam
ATP1A2 mutations in 11 families with familial hemiplegic migraine
✍ Florence Riant; Maurizio De Fusco; Paolo Aridon; Anne Ducros; Claire Ploton; Flo 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 497 KB

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