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Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation

โœ Scribed by Yee-Cheun Chan; Jean-Marc Burgunder; Einar Wilder-Smith; Soh-Eng Chew; Karen M.J. Lam-Mok-Sing; Vijay Sharma; Benjamin K.C. Ong


Book ID
116674201
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
758 KB
Volume
15
Category
Article
ISSN
0967-5868

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The novel p.L1649Q mutation in the SCN1A
โœ Kaate R.J. Vanmolkot; Elena Babini; Boukje de Vries; Anine H. Stam; Tobias Freil ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 492 KB

Familial hemiplegic migraine (FHM) is a severe subtype of migraine with hemiparesis during attacks. We scanned 10 families with FHM without mutations in the CACNA1A (FHM1) and ATP1A2 (FHM2) genes. We identified the novel p.L1649Q mutation (c.4946T>A) in Na(v)1.1 sodium channel gene SCN1A (FHM3) in a