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Article

Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred.

Neurogenetics - 1 Jul 2009

Cuenca-León Ester, Corominas Roser, Montfort Magda, Artigas Josep, Roig Manuel, Bayés Mònica, Cormand Bru, Macaya Alfons

Abstract excerpt

We sought to map the disease-causing gene in a large Spanish kindred with familial hemiplegic migraine (FHM). Patients were classified according to the ICHD-II criteria. After ruling out linkage to known migraine genetic loci, a single nucleotide polymorphism-based, 0.62-cM density genome-wide scan was performed. Among 13 affected subjects, FHM was the prevailing migraine phenotype in six, migraine with aura in...

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Source

Identifiers

PMID: 19153782
DOI: 10.1007/s10048-008-0169-6

Genes

ATXN3
ITPK1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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