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Migraine with aura as the predominant phenotype in a family with aPRRT2mutation

✍ Scribed by Una-Marie Sheerin, Maria Stamelou, Gavin Charlesworth…


Book ID
120898440
Publisher
Springer
Year
2012
Tongue
English
Weight
203 KB
Volume
260
Category
Article
ISSN
0340-5354

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✍ 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