A Recurrent de Novo Mutation in Kcnc1 Causes Progressive Myoclonus Epilepsy

AuthID
 P-00A-3Q4
51
Author(s)
Muona, M
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Berkovic, SF
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Document Type
Article
Year published
2015
Published
in NATURE GENETICS, ISSN: 1061-4036
Volume: 47, Issue: 1, Pages: 39-+ (11)
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Scopus®
Crossref®229
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Publication Identifiers
Pubmed: 25401298
Scopus: 2-s2.0-84930946843
Wos: WOS:000346990400009
Source Identifiers
ISSN: 1061-4036
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All authors
Name Order Nome   Name Order Nome   Name Order Nome
1 Muona, M;   2 Berkovic, SF;   3 Dibbens, LM;
4 Oliver, KL;   5 Maljevic, S;   6 Bayly, MA;
7 Joensuu, T;   8 Canafoglia, L;   9 Franceschetti, S;
10 Michelucci, R;   11 Markkinen, S;   12 Heron, SE;
13 Hildebrand, MS;   14 Andermann, E;   15 Andermann, F;
16 Gambardella, A;   17 Tinuper, P;   18 Licchetta, L;
19 Scheffer, IE;   20 Criscuolo, C;   21 Filla, A;
22 Ferlazzo, E;   23 Ahmad, J;   24 Ahmad, A;
25 Baykan, B;   26 Said, E;   27 Topcu, M;
28 Riguzzi, P;   29 King, MD;   30 Ozkara, C;
31 Andrade, DM;   32 Engelsen, BA;   33 Crespel, A;
34 Lindenau, M;   35 Lohmann, E;   36 Saletti, V;
37 Massano, J ;   38 Privitera, M;   39 Espay, AJ;
40 Kauffmann, B;   41 Duchowny, M;   42 Moller, RS;
43 Straussberg, R;   44 Afawi, Z;   45 Ben Zeev, B;
46 Samocha, KE;   47 Daly, MJ;   48 Petrou, S;
49 Lerche, H;   50 Palotie, A;   51 Lehesjoki, AE;

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