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pro vyhledávání: '"Neville, B. (B.)"'
Autor:
Marini, C. (C.), Mei, D. (D.), Temudo, T. (T.), Ferrari, A.R. (A. R.), Buti, D. (D.), Bonanni, P. (P.), Dravet, C. (C.), Dias, I.A. (I. A.), Moreira, A. (A.), Calado, E. (E.), Seri, S. (S.), Neville, B. (B.), Narbona, J. (Juan), Reid, E. (E.), Michelucci, R. (R.), Sicca, F. (F.), Cross, H. (H.), Guerrini, R. (R.)
Publikováno v:
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
instname
Purpose: Mutations in the genes coding for subunits of ion channels have been associated with epilepsy. Of these known epilepsy genes SCN1A, coding for the α subunit of the sodium channel, is currently the most clinically relevant gene. The majority
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dd73e2484c40da5156e4158dfcfe0785
https://hdl.handle.net/10171/57777
https://hdl.handle.net/10171/57777
