Article
Calcium channel mutations and migraine.
Current opinion in neurology - 1 Jun 2002
Kors Esther E, van den Maagdenberg Arn M J M, Plomp Jaap J, Frants Rune R, Ferrari Michel D
Abstract excerpt
An increasing number of mutations in the CACNA1A gene have been identified, which are associated with a broad clinical spectrum, including familial hemiplegic migraine. Transfection studies and mouse model analyses are currently being undertaken to study the correlation between CACNA1A mutations and disease.
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