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Article

A novel ATP1A2 mutation in a family with FHM type II.

Cephalalgia : an international journal of headache - 1 Mar 2006

Pierelli F, Grieco G S, Pauri F, Pirro C, Fiermonte G, Ambrosini A, Costa A, Buzzi M G, Valoppi M, Caltagirone C, Nappi G, Santorelli F M

Abstract excerpt

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura with an autosomal dominant pattern of inheritance. Six FHM families underwent extensive clinical and genetic investigation. The authors identified a novel ATP1A2 mutation (E700K) in three patients from one family. In the p...

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Identifiers

PMID: 16472340
DOI: 10.1111/j.1468-2982.2006.01002.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-16472340-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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