Pubblicazioni

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

2015 - AMERICAN JOURNAL OF HUMAN GENETICS

Dazzo, Emanuela; Fanciulli, Manuela; Serioli, Elena; Minervini, Giovanni; Pulitano, Patrizia; Binelli, Simona; Di Bonaventura, Carlo; Luisi, Concetta; Pasini, Elena; Striano, Salvatore; Striano, Pasquale; Coppola, Giangennaro; Chiavegato, Angela; Radovic, Slobodanka; Spadotto, Alessandro; Uzzau, Sergio; La Neve, Angela; Giallonardo, Anna Teresa; Mecarelli, Oriano; Tosatto, Silvio C. E; Ottman, Ruth; Michelucci, Roberto; Nobile, Carlo

Differentiation of IncL and IncM plasmids associated with the spread of clinically relevant antimicrobial resistance

2015 - PLOS ONE

Carattoli, A; Seiffert S., N; Schwendener, S; Perreten, V; Endimiani, A

Keppen-lubinsky syndrome is caused by mutations in the inwardly rectifying K+ channel encoded by KCNJ6

2015 - AMERICAN JOURNAL OF HUMAN GENETICS

Masotti, Andrea; Uva, Paolo; Davis Keppen, Laura; Basel Vanagaite, Lina; Cohen, Lior; Pisaneschi, Elisa; Celluzzi, Antonella; Bencivenga, Paola; Fang, Mingyan; Tian, Mingyu; Xu, Xun; Cappa, Marco; Dallapiccola, Bruno