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Hemiplegic migraine with reversible cerebral vasoconstriction caused byATP1A2mutations

✍ Scribed by Andreas Hermann, Kay Engelandt, Bernd Rautenstrauss…

Book ID
120898648
Publisher
Springer
Year
2013
Tongue
English
Weight
262 KB
Volume
260
Category
Article
ISSN
0340-5354

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ATP1A2 mutations in 11 families with fam
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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