The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

R. Michelucci, P. Pulitano, C. Di Bonaventura, S. Binelli, C. Luisi, E. Pasini, S. Striano, P. Striano, G. Coppola, A. La Neve, A.T. Giallonardo, O. Mecarelli, E. Serioli, E. Dazzo, M. Fanciulli, C. Nobile

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