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Article

A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.

Archives of neurology - 1 Jul 2008

Striano Pasquale, de Falco Arturo, Diani Erica, Bovo Giorgia, Furlan Sandra, Vitiello Libero, Pinardi Federica, Striano Salvatore, Michelucci Roberto, de Falco Fabrizio Antonio, Nobile Carlo

Abstract excerpt

BACKGROUND: Mutations responsible for autosomal dominant lateral temporal epilepsy have been found in the leucine-rich, glioma-inactivated 1 (LGI1) gene. OBJECTIVES: To describe the clinical and genetic findings in a family with autosomal dominant lateral temporal epilepsy and to determine the fu...

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Source

Identifiers

PMID: 18625862
DOI: 10.1001/archneur.65.7.939

Genes

LGI1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18625862-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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