Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants

Claudia Cuccurullo*, Emanuele Cerulli Irelli, Lorenzo Ugga, Antonella Riva, Alessandra D'Amico, Sara Cabet, Gaetan Lesca, Leonilda Bilo, Federico Zara, Catrinel Iliescu, Diana Barca, France Fung, Katherine Helbig, Xilma Ortiz-Gonzalez, Helenius J. Schelhaas, Marjolein H. Willemsen, Inge van der Linden, Laura Canafoglia, Carolina Courage, Samuele GommaraschiPedro Gonzalez-Alegre, Tanya Bardakjian, Steffen Syrbe, Elisabeth Schuler, Johannes R. Lemke, Stella Vari, Gitte Roende, Mads Bak, Mahbulul Huq, Zoe Powis, Katrine M. Johannesen, Trine Bjørg Hammer, Rikke S. Møller, Rachel Rabin, John Pappas, Mary L. Zupanc, Neda Zadeh, Julie Cohen, Sakkubai Naidu, Ilona Krey, Russell Saneto, Jenny Thies, Laura Licchetta, Paolo Tinuper, Francesca Bisulli, Raffaella Minardi, Allan Bayat, Nathalie Villeneuve, Florence Molinari, Hormos Salimi Dafsari, Birk Moller, Marie Le Roux, Clara Houdayer, Marilena Vecchi, Isabella Mammi, Elena Fiorini, Jacopo Proietti, Sofia Ferri, Gaetano Cantalupo, Domenica Immacolata Battaglia, Maria Luigia Gambardella, Ilaria Contaldo, Claudia Brogna, Marina Trivisano, Angela De Dominicis, Stefania Maria Bova, Elena Gardella, Pasquale Striano, Antonietta Coppola*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Biochemistry, Genetics and Molecular Biology