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RecurrentATP1A2mutations in Portuguese families with familial hemiplegic migraine

✍ Scribed by Maria-José Castro; Anine H. Stam; Carolina Lemos; José Barros; Raquel G. Gouveia; Isabel Pavão Martins; Jan B. Koenderink; Kaate R. J. Vanmolkot; Alexandre P. Mendes; Rune R. Frants; Michel D. Ferrari; Jorge Sequeiros; José M. Pereira-Monteiro; Arn M. J. M. van den Maagdenberg


Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
269 KB
Volume
52
Category
Article
ISSN
1435-232X

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ATP1A2 mutations in 11 families with fam
✍ 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