Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy

An Italian family with familial hemiplegic migraine (FHM) with the absence of mutations in the known genes associated with this disorder, namely ATP1A2, ATP1A3, CACNA1A, and SCN1A, has recently been reported. Soon afterward, whole exome sequencing allowed the identification of the carrier status of...

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Detalles Bibliográficos
Autores principales: Coppola, Giangennaro, Pastorino, Grazia Maria Giovanna, Vetri, Luigi, D’Onofrio, Floriana, Operto, Francesca Felicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349335/
https://www.ncbi.nlm.nih.gov/pubmed/32549268
http://dx.doi.org/10.3390/brainsci10060372

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349335/
https://www.ncbi.nlm.nih.gov/pubmed/32549268
http://dx.doi.org/10.3390/brainsci10060372

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