Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleNew ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy.AuthorsMartín-Hernández, Elena; Rodríguez-García, María; Camacho, Ana; Matilla-Dueñas, Antoni; García-Silva, María; Quijada-Fraile, Pilar; Corral-Juan, Marc; Tejada-Palacios, Pilar; Las Heras, Rogelio; Arenas, Joaquín; Martín, Miguel; Martínez-Azorín, FranciscoPublicationNeurogenetics, 2016, Vol 17, Issue 4, p259ISSN1364-6745Publication typeArticleDOI10.1007/s10048-016-0496-y