Publicacións en colaboración con investigadores/as de Radboud University Nijmegen Medical Centre (2)

2008

  1. Two novel functional mutations in the Na+, K+ -ATPase α2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes

    Clinical Genetics, Vol. 73, Núm. 1, pp. 37-43

2007

  1. Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine

    Journal of Human Genetics, Vol. 52, Núm. 12, pp. 990-998