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EHMTI-0187. A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer
2014
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Materias: | |
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 |
description | |
format | Online Article Text |
id | pubmed-4180365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer |
record_format | MEDLINE/PubMed |
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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