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Article

De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report.

The journal of headache and pain - 1 Dec 2017

Gagliardi Stella, Grieco Gaetano Salvatore, Gualandi Francesca, Caniatti Luisa Maria, Groppo Elisabetta, Valente Marialuisa, Nappi Giuseppe, Neri Marcella, Cereda Cristina

Abstract excerpt

BACKGROUND: Sporadic Hemiplegic Migraine is a rare form of migraine headache. Mutations in three different genes, two ion-channel genes and one encoding an ATP exchanger, CACNA1A, ATP1A2 and SCN1A are all responsible for the FHM phenotype, thus indicating a genetic heterogeneity for this disorder. Here, we described a de novo exonic duplication of ATP1A2 in an Italian patient with Hemiplegic Migraine. CASE...

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Identifiers

PMID: 28593511
DOI: 10.1186/s10194-017-0770-x
PMCID: PMC5462664

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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