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Article

A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy.

Seizure - 1 Jan 2014

Lee Moon Kyu, Kim So Won, Lee Ji Hyun, Cho Yang-Je, Kim Doh-Eui, Lee Byung In, Kim Ho Min, Lee Min Goo, Heo Kyoung

Abstract excerpt

PURPOSE: A new leucine-rich glioma-inactivated 1 gene (LGI1) mutation inducing an amino acid sequence substitution was found in a Korean family with autosomal dominant lateral temporal lobe epilepsy (ADLTE). We report the clinical features and characteristics of this newly identified LGI1 mutation. METHODS: Clinical data were collected from a large ADLTE family. All exons and flanking regions of the LGI1 gene...

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Source

Identifiers

PMID: 24177143
DOI: 10.1016/j.seizure.2013.10.001

Genes

LGI1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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