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

Detalles Bibliográficos
Autores principales: Martínez, E, Moreno, R, López-Mesonero, L, Ruiz, M, Vidriales, I, Mulero, P, Téllez, N, Guerrero, A, Tellería, JJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Meeting Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180365/
http://dx.doi.org/10.1186/1129-2377-15-S1-B12
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author Martínez, E
Moreno, R
López-Mesonero, L
Ruiz, M
Vidriales, I
Mulero, P
Téllez, N
Guerrero, A
Tellería, JJ
author_facet Martínez, E
Moreno, R
López-Mesonero, L
Ruiz, M
Vidriales, I
Mulero, P
Téllez, N
Guerrero, A
Tellería, JJ
author_sort Martínez, E
collection PubMed
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spelling pubmed-41803652014-10-02 EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks Martínez, E Moreno, R López-Mesonero, L Ruiz, M Vidriales, I Mulero, P Téllez, N Guerrero, A Tellería, JJ J Headache Pain Meeting Abstract Springer 2014 2014-09-18 /pmc/articles/PMC4180365/ http://dx.doi.org/10.1186/1129-2377-15-S1-B12 Text en Copyright © 2014 Martínez et al; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Meeting Abstract
Martínez, E
Moreno, R
López-Mesonero, L
Ruiz, M
Vidriales, I
Mulero, P
Téllez, N
Guerrero, A
Tellería, JJ
EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
title EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
title_full EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
title_fullStr EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
title_full_unstemmed EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
title_short EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
title_sort ehmti-0187. a novel atp1a2 mutation in a case of familial hemiplegic migraine with especially severe attacks
topic Meeting Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180365/
http://dx.doi.org/10.1186/1129-2377-15-S1-B12
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