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

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. H...

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Detalles Bibliográficos
Autores principales: Gagliardi, Stella, Grieco, Gaetano Salvatore, Gualandi, Francesca, Caniatti, Luisa Maria, Groppo, Elisabetta, Valente, Marialuisa, Nappi, Giuseppe, Neri, Marcella, Cereda, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462664/
https://www.ncbi.nlm.nih.gov/pubmed/28593511
http://dx.doi.org/10.1186/s10194-017-0770-x

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