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Genetic Analysis of a Large Family with Migraine, Vertigo, and Motion Sickness.

Dopamine-beta-hydroxylase 19-bp insertion/deletion polymorphism affects medication overuse in patients with chronic migraine

Association between PRDM16, MEF2D, TRPM8, LRP1 gene polymorphisms and migraine susceptibility in the She ethnic population in China.

Migraine-associated gene expression in cell types of the central and peripheral nervous system

rs2651899 variant is associated with risk for migraine without aura from North Indian population

Current understanding of cortical structure and function in migraine

Could rs4379368 be a genetic marker for North Indian migraine patients with aura?: Preliminary evidence by a replication study

TRPM8 genetic variant is associated with chronic migraine and allodynia

C677T Methylenetetrahydrofolate Reductase Homozygosis and Vitamin Supplement in Migraineur Children

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Migraine Susceptibility 편두통 감수성

Migraine Susceptibility 편두통 감수성
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