APA
Oliver K. L., Franceschetti S., Milligan C. J., Muona M., Mandelstam S. A., Canafoglia L., Boguszewska-Chachulska A. M., Korczyn A. D., Bisulli F., Di Bonaventura C., Ragona F., Michelucci R., Ben-Zeev B., Straussberg R., Panzica F., Massano J., Friedman D., Crespel A., Engelsen B. A., Andermann F., Andermann E., Spodar K., Lasek-Bal A., Riguzzi P., Pasini E., Tinuper P., Licchetta L., Gardella E., Lindenau M., Wulf A., Møller R. S., Benninger F., Afawi Z., Rubboli G., Reid C. A., Maljevic S., Lerche H., Lehesjoki A., Petrou S. & Berkovic S. F. (20170719). Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K. : Annals of neurology.
Chicago
Oliver Karen L, Franceschetti Silvana, Milligan Carol J, Muona Mikko, Mandelstam Simone A, Canafoglia Laura, Boguszewska-Chachulska Anna M, Korczyn Amos D, Bisulli Francesca, Di Bonaventura Carlo, Ragona Francesca, Michelucci Roberto, Ben-Zeev Bruria, Straussberg Rachel, Panzica Ferruccio, Massano João, Friedman Daniel, Crespel Arielle, Engelsen Bernt A, Andermann Frederick, Andermann Eva, Spodar Krystyna, Lasek-Bal Anetta, Riguzzi Patrizia, Pasini Elena, Tinuper Paolo, Licchetta Laura, Gardella Elena, Lindenau Matthias, Wulf Annette, Møller Rikke S, Benninger Felix, Afawi Zaid, Rubboli Guido, Reid Christopher A, Maljevic Snezana, Lerche Holger, Lehesjoki Anna-Elina, Petrou Steven and Berkovic Samuel F. 20170719. Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K. : Annals of neurology.
Harvard
Oliver K. L., Franceschetti S., Milligan C. J., Muona M., Mandelstam S. A., Canafoglia L., Boguszewska-Chachulska A. M., Korczyn A. D., Bisulli F., Di Bonaventura C., Ragona F., Michelucci R., Ben-Zeev B., Straussberg R., Panzica F., Massano J., Friedman D., Crespel A., Engelsen B. A., Andermann F., Andermann E., Spodar K., Lasek-Bal A., Riguzzi P., Pasini E., Tinuper P., Licchetta L., Gardella E., Lindenau M., Wulf A., Møller R. S., Benninger F., Afawi Z., Rubboli G., Reid C. A., Maljevic S., Lerche H., Lehesjoki A., Petrou S. and Berkovic S. F. (20170719). Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K. : Annals of neurology.
MLA
Oliver Karen L, Franceschetti Silvana, Milligan Carol J, Muona Mikko, Mandelstam Simone A, Canafoglia Laura, Boguszewska-Chachulska Anna M, Korczyn Amos D, Bisulli Francesca, Di Bonaventura Carlo, Ragona Francesca, Michelucci Roberto, Ben-Zeev Bruria, Straussberg Rachel, Panzica Ferruccio, Massano João, Friedman Daniel, Crespel Arielle, Engelsen Bernt A, Andermann Frederick, Andermann Eva, Spodar Krystyna, Lasek-Bal Anetta, Riguzzi Patrizia, Pasini Elena, Tinuper Paolo, Licchetta Laura, Gardella Elena, Lindenau Matthias, Wulf Annette, Møller Rikke S, Benninger Felix, Afawi Zaid, Rubboli Guido, Reid Christopher A, Maljevic Snezana, Lerche Holger, Lehesjoki Anna-Elina, Petrou Steven and Berkovic Samuel F. Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K. : Annals of neurology. 20170719.