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Article

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

Epilepsy & behavior : E&B - 1 Mar 2017

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

Abstract excerpt

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, collected by epileptologists participating in a collaborative study of the Commission for Genetics of the Italian...

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Source

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Identifiers

PMID: 28142128
DOI: 10.1016/j.yebeh.2016.12.003
PMCID: PMC5378904

Genes

RELN
LGI1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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