Published in
Springer (part of Springer Nature), neurogenetics, 4(17), p. 259-263
DOI: 10.1007/s10048-016-0496-y
Links
Tools
New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy
Journal article published in 2016 by
Elena Martín-Hernández,
María Elena Rodríguez-García,
Ana Camacho,
Antoni Matilla-Dueñas,
María Teresa García-Silva,
Pilar Quijada-Fraile,
Marc Corral-Juan,
Pilar Tejada-Palacios,
Rogelio Simón de Las Heras,
Joaquín Arenas 
,
Miguel A. Martín,
Francisco Martínez-Azorín
,
Miguel A. Martín,
Francisco Martínez-Azorín
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 