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Article

A new locus for hemiplegic migraine maps to chromosome 1q31.

Neurology - 1 Nov 1997

Gardner K, Barmada M M, Ptacek L J, Hoffman E P

Abstract excerpt

A single familial hemiplegic migraine locus has been previously mapped to 19p13.1 and associated with mutations in a calcium channel gene (CACNL1A4). We describe a new 39-member four-generation family from Wyoming of German-Native American descent with autosomal dominant familial hemiplegic migraine that is not linked to the chromosome 19p locus. Affected individuals showed a stereotypic pattern of migrainous...

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Identifiers

PMID: 9371899
DOI: 10.1212/wnl.49.5.1231

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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A new locus for hemiplegic migraine maps to chromosome 1q31.PMID 9371899Read ↗

Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneitySemantic proximity Read ↗

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The molecular genetics of migraine.Semantic proximity Read ↗

Current status of genetic discoveries in migraine: familial hemiplegic migraine and beyond.Semantic proximity Read ↗

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.Semantic proximity Read ↗

Familial hemiplegic migraine: a ion channel disorder.Semantic proximity Read ↗

Recent findings in headache genetics.Semantic proximity Read ↗

Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation.Semantic proximity Read ↗

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.Semantic proximity Read ↗

Familial hemiplegic migraine.Semantic proximity Read ↗

A typical migraine susceptibility region localizes to chromosome 1q31.Semantic proximity Read ↗

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.Semantic proximity Read ↗

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