Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations
โ Scribed by Michelucci, Roberto; Pasini, Elena; Malacrida, Sandro; Striano, Pasquale; Bonaventura, Carlo Di; Pulitano, Patrizia; Bisulli, Francesca; Egeo, Gabriella; Santulli, Lia; Sofia, Vito; Gambardella, Antonio; Elia, Maurizio; de Falco, Arturo; Neve, Angela la; Banfi, Paola; Coppola, Giangennaro; Avoni, Patrizia; Binelli, Simona; Boniver, Clementina; Pisano, Tiziana; Marchini, Marco; Dazzo, Emanuela; Fanciulli, Manuela; Bartolini, Yerma; Riguzzi, Patrizia; Volpi, Lilia; de Falco, Fabrizio A.; Giallonardo, Anna Teresa; Mecarelli, Oriano; Striano, Salvatore; Tinuper, Paolo; Nobile, Carlo
- Book ID
- 120312091
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2013
- Tongue
- English
- Weight
- 258 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0013-9580
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Autosomal dominant lateral temporal epilepsy (ADLTE) or autosomal dominant partial epilepsy with auditory features (ADPEAF) is an inherited epileptic syndrome with onset in childhood/adolescence and benign evolution. The hallmark of the syndrome consists of typical auditory auras or ictal aphasia in