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Article

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.

Annals of neurology - 1 Mar 2003

Marconi Roberto, De Fusco Maurizio, Aridon Paolo, Plewnia Katrin, Rossi Maja, Carapelli Sadia, Ballabio Andrea, Morgante Letterio, Musolino Rosa, Epifanio Antonio, Micieli Giuseppe, De Michele Giuseppe, Casari Giorgio

Abstract excerpt

Familial hemiplegic migraine (FHM) is a rare autosomal dominant disorder characterized by episodes of transient hemiparesis followed by headache. Two chromosomal loci are associated to FHM: FHM1 on chromosome 19 and FHM2 on chromosome 1q21-23. Mutations of the alpha-1A subunit of the voltage gate...

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PMID: 12601705
DOI: 10.1002/ana.10464

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-12601705-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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