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| Title : PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy - Hildebrand_2015_Ann.Clin.Transl.Neurol_2_821 |
| Author(s) : Hildebrand MS , Tankard R , Gazina EV , Damiano JA , Lawrence KM , Dahl HH , Regan BM , Shearer AE , Smith RJ , Marini C , Guerrini R , Labate A , Gambardella A , Tinuper P , Lichetta L , Baldassari S , Bisulli F , Pippucci T , Scheffer IE , Reid CA , Petrou S , Bahlo M , Berkovic SF |
| Ref : Ann Clin Transl Neurol , 2 :821 , 2015 |
| Abstract : Hildebrand_2015_Ann.Clin.Transl.Neurol_2_821 |
| ESTHER : Hildebrand_2015_Ann.Clin.Transl.Neurol_2_821 |
| PubMedSearch : Hildebrand_2015_Ann.Clin.Transl.Neurol_2_821 |
| PubMedID: 26339676 |
| Title : Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20 - Knight_2004_Brain_127_1172 |
| Author(s) : Knight MA , Gardner RJ , Bahlo M , Matsuura T , Dixon JA , Forrest SM , Storey E |
| Ref : Brain , 127 :1172 , 2004 |
| Abstract : Knight_2004_Brain_127_1172 |
| ESTHER : Knight_2004_Brain_127_1172 |
| PubMedSearch : Knight_2004_Brain_127_1172 |
| PubMedID: 14998916 |
| Gene_locus related to this paper: human-DAGLA |