A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Authors
Mikko Muona,
Samuel BerkovicLeanne Dibbens,
Karen Oliver,
Snezana Maljevic,
Marta Bayly,
Tarja Joensuu,
Laura Canafoglia,
Silvana Franceschetti,
Roberto Michelucci,
Salla Markkinen,
Sarah Heron,
Michael Hildebrand,
Eva Andermann,
Frédérick Andermann,
Antonio Gambardella,
Paolo Tinuper,
Laura Licchetta,
Ingrid Scheffer,
Chiara Criscuolo,
Alessandro Filla,
Edoardo Ferlazzo,
Jamil Ahmad,
Adeel Ahmad,
Betül Baykan,
Edith Said,
Meral Topçu,
P. Riguzzi,
Mary King,
Çiğdem Özkara,
Danielle Andrade,
Bernt Engelsen,
Arielle Crespel,
Matthias Lindenau,
Ebba Lohmann,
Veronica Saletti,
João Massano,
Michael Privitera,
Alberto Espay,
Brice Kauffmann,
Michael Duchowny,
Rikke Møller,
Rachel Straussberg,
Zaid Afawi,
Bruria Ben‐Zeev,
Kaitlin Samocha,
Mark Daly,
Steven Petrou,
Holger Lerche,
Aarno Palotie +48 authors
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Anna-Elina Lehesjoki Tip Tip