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Acetazolamide responsiveness in familial hemiplegic migraine

โœ Scribed by B. S. Athwal; G. G. Lennox

Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
187 KB
Volume
40
Category
Article
ISSN
0364-5134

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๐Ÿ“œ SIMILAR VOLUMES

ATP1A2 mutations in 11 families with fam
ATP1A2 mutations in 11 families with familial hemiplegic migraine
โœ Florence Riant; Maurizio De Fusco; Paolo Aridon; Anne Ducros; Claire Ploton; Flo ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 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