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Two novel SCN1A mutations identified in families with familial hemiplegic migraine

✍ Scribed by Weller, C. M.; Pelzer, N.; de Vries, B.; Lopez, M. A.; De Fabregues, O.; Pascual, J.; Arroyo, M. A. R.; Koelewijn, S. C.; Stam, A. H.; Haan, J.; Ferrari, M. D.; Terwindt, G. M.; van den Maagdenberg, A. M.

Book ID
121808803
Publisher
John Wiley and Sons
Year
2014
Tongue
English
Weight
346 KB
Volume
34
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 πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 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