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Article

Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study.

Cephalalgia : an international journal of headache - 1 Feb 2006

Schwaag S, Evers S, Schirmacher A, Stögbauer F, Ringelstein E B, Kuhlenbäumer G

Abstract excerpt

Mutations in the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Exons 3 and 4 are mutation hotspots. Migraine is a clinical hallmark of CADASIL. The objective of this study was to investigate whether genetic variants in exons 3 and 4 of the NOTCH3 gene are associated with migraine. Exons 3 and 4 of the NOTCH3 were analysed for mutations and...

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Source

Identifiers

PMID: 16426270
DOI: 10.1111/j.1468-2982.2005.01007.x

Genes

NOTCH3

Provenance

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.

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