Skip to main content
Top
Published in: The Journal of Headache and Pain 1/2014

Open Access 01-12-2014 | Meeting abstract

EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks

Authors: E Martínez, R Moreno, L López-Mesonero, M Ruiz, I Vidriales, P Mulero, N Téllez, A Guerrero, JJ Tellería

Published in: The Journal of Headache and Pain | Special Issue 1/2014

Login to get access

Excerpt

Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during aura phase. Mutations in CACNA1A, ATP1A2, SCN1A and PRRT2 genes have been described. …
Metadata
Title
EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
Authors
E Martínez
R Moreno
L López-Mesonero
M Ruiz
I Vidriales
P Mulero
N Téllez
A Guerrero
JJ Tellería
Publication date
01-12-2014
Publisher
Springer Milan
Published in
The Journal of Headache and Pain / Issue Special Issue 1/2014
Print ISSN: 1129-2369
Electronic ISSN: 1129-2377
DOI
https://doi.org/10.1186/1129-2377-15-S1-B12

Other articles of this Special Issue 1/2014

The Journal of Headache and Pain 1/2014 Go to the issue