KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum / Bonardi, Cm; Heyne, Ho; Fiannacca, M; Fitzgerald, Mp; Gardella, E; Gunning, B; Olofsson, K; Lesca, G; Verbeek, N; Stamberger, H; Striano, P; Zara, F; Mancardi, Mm; Nava, C; Syrbe, S; Buono, S; Baulac, S; Coppola, A; Weckhuysen, S; Schoonjans, As; Ceulemans, B; Sarret, C; Baumgartner, T; Muhle, H; des Portes, V; Toulouse, J; Nougues, Mc; Rossi, M; Demarquay, G; Ville, D; Hirsch, E; Maurey, H; Willems, M; de Bellescize, J; Altuzarra, Cd; Villeneuve, N; Bartolomei, F; Picard, F; Hornemann, F; Koolen, Da; Kroes, Hy; Reale, C; Fenger, Cd; Tan, Wh; Dibbens, L; Bearden, Dr; Møller, Rs; Rubboli, G.. - In: BRAIN. - ISSN 0006-8950. - 144:(2021), pp. 3635-3650. [10.1093/brain/awab219]

KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum.

Striano P;Coppola A;Hirsch E;Bartolomei F;
2021

2021
KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum / Bonardi, Cm; Heyne, Ho; Fiannacca, M; Fitzgerald, Mp; Gardella, E; Gunning, B; Olofsson, K; Lesca, G; Verbeek, N; Stamberger, H; Striano, P; Zara, F; Mancardi, Mm; Nava, C; Syrbe, S; Buono, S; Baulac, S; Coppola, A; Weckhuysen, S; Schoonjans, As; Ceulemans, B; Sarret, C; Baumgartner, T; Muhle, H; des Portes, V; Toulouse, J; Nougues, Mc; Rossi, M; Demarquay, G; Ville, D; Hirsch, E; Maurey, H; Willems, M; de Bellescize, J; Altuzarra, Cd; Villeneuve, N; Bartolomei, F; Picard, F; Hornemann, F; Koolen, Da; Kroes, Hy; Reale, C; Fenger, Cd; Tan, Wh; Dibbens, L; Bearden, Dr; Møller, Rs; Rubboli, G.. - In: BRAIN. - ISSN 0006-8950. - 144:(2021), pp. 3635-3650. [10.1093/brain/awab219]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/854937
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