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 <i>ATP1A2</i>, <i>ATP1A3</i>, <i>CACNA1A</i>, and <i>SCN1A</i>, has recently been reported. Soon afterward,...

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Bibliographic Details
Main Authors: Giangennaro Coppola, Grazia Maria Giovanna Pastorino, Luigi Vetri, Floriana D’Onofrio, Francesca Felicia Operto
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Brain Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3425/10/6/372