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Article

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

3 Dec 2007

Abstract excerpt

BACKGROUND: Familial (FHM) and sporadic (SHM) hemiplegic migraine are severe subtypes of migraine associated with transient hemiparesis. For FHM, three genes have been identified encoding subunits of a calcium channel (CACNA1A), a sodium-potassium pump (ATP1A2), and a sodium channel (SCN1A). Their role in SHM is unknown. Establishing a genetic basis for SHM may further the understanding of its pathophysiology and...

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PMID: 18056581
DOI: 10.1212/01.wnl.0000295670.01629.5a

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