Myoclonus Epilepsy and Ataxia due to KCNC1 Mutation : Analysis of 20 Cases and K plus Channel Properties

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Myoclonus Epilepsy and Ataxia due to KCNC1 Mutation : Analysis of 20 Cases and K plus Channel Properties

Author: 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, Joao; 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; Moller, Rikke S.; Benninger, Felix; Afawi, Zaid; Rubboli, Guido; Reid, Christopher A.; Maljevic, Snezana; Lerche, Holger; Lehesjoki, Anna-Elina; Petrou, Steven; Berkovic, Samuel F.
Tübinger Autor(en):
Maljevic, Snezana
Lerche, Holger
Published in: Annals of Neurology (2017), Bd. 81, H. 5, S. 677-689
Verlagsangabe: Wiley
Language: English
Full text: http://dx.doi.org/10.1002/ana.24929
ISSN: 1531-8249
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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