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

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

Abstract 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 dis...

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Bibliographic Details
Main Authors: Stella Gagliardi, Gaetano Salvatore Grieco, Francesca Gualandi, Luisa Maria Caniatti, Elisabetta Groppo, Marialuisa Valente, Giuseppe Nappi, Marcella Neri, Cristina Cereda
Format: Article
Language:English
Published: BMC 2017-06-01
Series:The Journal of Headache and Pain
Subjects:
ATP1A2
Duplication
Hemiplegic migraine
De novo
Online Access:http://link.springer.com/article/10.1186/s10194-017-0770-x

Internet

http://link.springer.com/article/10.1186/s10194-017-0770-x

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