Molecular genetics of migraine headaches: a review

被引:74
作者
Montagna, P [1 ]
机构
[1] Univ Bologna, Sch Med, Inst Clin Neurol, I-40123 Bologna, Italy
关键词
migraine; genetics; calcium channels; familial hemiplegic migraine;
D O I
10.1046/j.1468-2982.2000.00003.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Following the recent discovery of neural calcium channel mutations in familial hemiplegic migraine, genetic linkage and association studies have been performed world-wide in an effort to unveil the genetic basis of the more common types of migraine too. Mutations in neural calcium channels, mitochondrial DNA, serotonin receptors and transporter, dopamine receptors and genetic prothrombotic risk factors have been especially investigated and are discussed here. No unambiguous conclusions have, however, been reached. FHM remains an isolated success story in the quest for the genetic basis of migraine.
引用
收藏
页码:3 / 14
页数:12
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