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

por Martínez, E, Moreno, R, López-Mesonero, L, Ruiz, M, Vidriales, I, Mulero, P, Téllez, N, Guerrero, A, Tellería, JJ
Publicado 2014