Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: First evidence for an altered channel regulation by syntaxin-1A / Soldovieri, Mv; Boutry Kryza, N; Milh, M; Doummar, D; Heron, B; Bourel, E; Ambrosino, P; Miceli, Francesco; De Maria, M; Dorison, N; Auvin, S; Echenne, B; Oertel, J; Riquet, A; Lambert, L; Gerard, M; Roubergue, A; Calender, A; Mignot, C; Taglialatela, Maurizio; Lesca, G.. - In: HUMAN MUTATION. - ISSN 1059-7794. - 35:3(2014), pp. 356-367. [10.1002/humu.22500]
Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: First evidence for an altered channel regulation by syntaxin-1A
MICELI, Francesco;TAGLIALATELA, MAURIZIO;
2014
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