Calcium channel mutations and migraine
- PMID: 12045730
- DOI: 10.1097/00019052-200206000-00014
Calcium channel mutations and migraine
Abstract
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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