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    Projects

    Research Output

    A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy

    Vetri, L., Calì, F., Vinci, M., Amato, C., Roccella, M., Granata, T., Freri, E., Solazzi, R., Romano, V. & Elia, M., Jan 1 2020, (Accepted/In press) In : European Journal of Medical Genetics. 103848.

    Research output: Contribution to journalArticle

  • Advances in genetic testing and optimization of clinical management in children and adults with epilepsy

    on the behalf of Genetic Commission of Italian League Against Epilepsy (LICE), Jan 1 2020, (Accepted/In press) In : Expert Review of Neurotherapeutics.

    Research output: Contribution to journalReview article

  • Open Access