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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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