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Article

Haplotype-based systematic association studies of ATP1A2 in migraine with aura.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Apr 2006

Netzer Christian, Todt Unda, Heinze Axel, Freudenberg Jan, Zumbroich Vera, Becker Tim, Goebel Ingrid, Ohlraun Stephanie, Goebel Hartmut, Kubisch Christian

Abstract excerpt

Mutations in ATP1A2 cause familial hemiplegic migraine (FHM) type 2, a rare monogenic form of migraine with aura (MA). Moreover, rare ATP1A2 missense variants are found in familial clustering of common forms of migraine in single pedigrees. To determine whether also common ATP1A2 polymorphisms co...

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Source

Identifiers

PMID: 16508935
DOI: 10.1002/ajmg.b.30283

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16508935-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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