Diagnostic implications of genetic copy number variation in epilepsy plus

Authors :: Coppola, A1
2, 3
Cellini, E4
Stamberger, H5
6, 7
Saarentaus, E8
9, 10
Cetica, V4
Lal, D10
11, 12
Djémié, T5
6
Bartnik-Glaska, M13
Ceulemans, B14
Cross, JH15
16, 17
Deconinck, T5
De Masi S7
Dorn, T18
Guerrini, R
Hoffman-Zacharska, D14
Kooy, F19
Lagae, L20
Lench, N21
Lemke, JR22
Lucenteforte, E23
Madia, F25
Mefford, HC26
Morrogh, D21
Nuernberg, P27
Palotie, A11
Schoonjans, AS15
Striano, P28
Szczepanik, E29
Tostevin, A1
2
Vermeesch, JR30
Van Esch H30
Van Paesschen W31
Waters, JJ21
Weckhuysen, S5
6, 12
Zara, F25
De Jonghe P5
Sisodiya, SM1
Marini, C
EuroEPINOMICS-RES, Consortium
Lehesjioki AE, EpiCNV Consortium.
Craiu, D
Talvik, T
Caglayan, H
Serratosa, J
Sterbova, K
Møller, Rs
Hjalgrim, H
Lerche, H
Weber, Y
Helbig, I
von Spiczak, S
Barba, C
Bogaerts, A
Boni, A
Galizia, Ec
Chiari, S
Di Gacomo, G
Ferrari, A
Garducci, S
Giglio, S
Holmgren, P
Leu, C
Melani, F
Novara, F
Pantaleo, M
Peeters, E
Pisano, T
Rosati, A
Sander, J
Schoeler, N
Stankiewicz, P
Striano, S
Suls, A
Traverso, M
Vandeweyer, G
Van Dijck, A
Zuffardi, O.
Publication Year :: 2019

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