Epilepsy with auditory features: A heterogeneous clinico-molecular disease

OBJECTIVE: To identify novel genes implicated in epilepsy with auditory features (EAF) in phenotypically heterogeneous families with unknown molecular basis. METHODS: We identified 15 probands with EAF in whom an LGI1 mutation had been excluded. We performed electroclinical phenotyping on all proban...

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Detalles Bibliográficos
Autores principales: Pippucci, Tommaso, Licchetta, Laura, Baldassari, Sara, Palombo, Flavia, Menghi, Veronica, D'Aurizio, Romina, Leta, Chiara, Stipa, Carlotta, Boero, Giovanni, d'Orsi, Giuseppe, Magi, Alberto, Scheffer, Ingrid, Seri, Marco, Tinuper, Paolo, Bisulli, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821078/
https://www.ncbi.nlm.nih.gov/pubmed/27066544
http://dx.doi.org/10.1212/NXG.0000000000000005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821078/
https://www.ncbi.nlm.nih.gov/pubmed/27066544
http://dx.doi.org/10.1212/NXG.0000000000000005

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