Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families.

doi:10.1046/j.1528-1157.2003.20003.x

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Article

Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families.

Epilepsia - 1 Oct 2003

Michelucci Roberto, Poza Juan Jose, Sofia Vito, de Feo Maria Rita, Binelli Simona, Bisulli Francesca, Scudellaro Evan, Simionati Barbara, Zimbello Rosanna, D'Orsi Giuseppe, Passarelli Daniela, Avoni Patrizia, Avanzini Giuliano, Tinuper Paolo, Biondi Roberto, Valle Giorgio, Mautner Victor F, Stephani Ulrich, Tassinari Carlo Alberto, Moschonas Nicholas K, Siebert Reiner, Lopez de Munain Adolpho, Perez-Tur Jordi, Nobile Carlo

Abstract excerpt

PURPOSE: [corrected] To describe the clinical and genetic findings of seven additional pedigrees with autosomal dominant lateral temporal epilepsy (ADLTE). METHODS: A personal and family history was obtained from each affected and unaffected member, along with a physical and neurologic examination. Routine and sleep EEGs, computed tomography (CT), or magnetic resonance imaging (MRI) were performed in almost all...

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Identifiers

PMID: 14510822
DOI: 10.1046/j.1528-1157.2003.20003.x

Genes

LGI1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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