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A novel missenseATP1A2mutation in a Finnish family with familial hemiplegic migraine type 2

✍ Scribed by M.A. Kaunisto; H. Harno; K.R.J. Vanmolkot; J.J. Gargus; G. Sun; E. Hämäläinen; E. Liukkonen; M. Kallela; A.M.J.M. Maagdenberg; R.R. Frants; M. Färkkilä; A. Palotie; M. Wessman

Publisher
Springer
Year
2004
Tongue
English
Weight
322 KB
Volume
5
Category
Article
ISSN
1364-6745

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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