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Article

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.

Human mutation - 1 Oct 2005

Todt Unda, Dichgans Martin, Jurkat-Rott Karin, Heinze Axel, Zifarelli Giovanni, Koenderink Jan B, Goebel Ingrid, Zumbroich Vera, Stiller Anne, Ramirez Alfredo, Friedrich Thomas, Göbel Hartmut, Kubisch Christian

Abstract excerpt

Migraine is a recurrent neurovascular disease. Its two most common forms-migraine without aura (MO) and migraine with aura (MA)-both show familial clustering and a complex pattern of inheritance. Familial hemiplegic migraine (FHM) is a rare monogenic subform caused by mutations in the calcium cha...

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Identifiers

PMID: 16110494
DOI: 10.1002/humu.20229

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16110494-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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