Publicaciones en colaboración con investigadores/as de University of Padua (3)

2003

  1. Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families

    Epilepsia, Vol. 44, Núm. 10, pp. 1289-1297

2002

  1. Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia

    Gene, Vol. 282, Núm. 1-2, pp. 87-94

  2. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

    Human Molecular Genetics, Vol. 11, Núm. 9, pp. 1119-1128