HCN1 mutation spectrum: From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

C. Marini, A. Porro, A. Rastetter, C. Dalle, I. Rivolta, D. Bauer, R. Oegema, C. Nava, E. Parrini, D. Mei, C. Mercer, R. Dhamija, C. Chambers, C. Coubes, J. Thévenon, P. Kuentz, S. Julia, L. Pasquier, C. Dubourg, W. CarréA. Rosati, F. Melani, T. Pisano, M. Giardino, A.M. Innes, Y. Alembik, S. Scheidecker, M. Santos, S. Figueiroa, C. Garrido, C. Fusco, D. Frattini, C. Spagnoli, A. Binda, T. Granata, F. Ragona, E. Freri, S. Franceschetti, L. Canafoglia, B. Castellotti, C. Gellera, R. Milanesi, M.M. Mancardi, D.R. Clark, F. Kok, K.L. Helbig, F. Zara, P. Striano, R. Guerrini, A. Moroni

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)3160-3178
Number of pages19
JournalBrain
Volume141
Issue number11
DOIs
Publication statusPublished - 2018

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