| Literature DB >> 12720601 |
Esther Kors1, Joost Haan, Michel Ferrari.
Abstract
The genetics of migraine is a fascinating and moving research area. Familial hemiplegic migraine, a rare subtype of migraine with a Mendelian pattern of inheritance, is caused by mutations in the chromosome 19 CACNA1A gene in approximately 75% of the families. The finding of mutations in an ionchannel subunit defines migraine as a channelopathy (eg, epilepsy). The genetics of the more frequent variants, migraine with and without aura, is more complex. Several loci have been studied in families and case-control studies, but need to be confirmed.Entities:
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Year: 2003 PMID: 12720601 DOI: 10.1007/s11916-003-0075-4
Source DB: PubMed Journal: Curr Pain Headache Rep ISSN: 1534-3081