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

OBJECTIVE: To describe the clinical phenotype of 7 families with Autosomal Dominant Lateral Temporal Lobe Epilepsy (ADLTE) related to Reelin (RELN) mutations comparing the data with those observed in 12 LGI1-mutated pedigrees belonging to our series. METHODS: Out of 40 Italian families with ADLTE, c...

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Bibliografiset tiedot
Julkaisussa:Epilepsy Behav
Päätekijät: Michelucci, Roberto, Pulitano, Patrizia, Di Bonaventura, Carlo, Binelli, Simona, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Serioli, Elena, Dazzo, Emanuela, Fanciulli, Manuela, Nobile, Carlo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Academic Press 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5378904/
https://ncbi.nlm.nih.gov/pubmed/28142128
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yebeh.2016.12.003
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