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Article

Kleine-Levin syndrome is associated with LMOD3 variants.

Journal of sleep research - 1 Jun 2019

Al Shareef Saad M, Basit Sulman, Li Sha, Pfister Corinne, Pradervand Sylvain, Lecendreux Michel, Mayer Geert, Dauvilliers Yves, Salpietro Vincenzo, Houlden Henry, BaHammam Ahmed S, Tafti Mehdi

Abstract excerpt

Kleine-Levin syndrome (KLS) is a rare periodic hypersomnia with associated behavioural abnormalities but with often favourable prognosis. There is excess risk of KLS in first-degree relatives, suggesting a strong genetic contribution. So far, no mutation is identified in KLS and comprehensive genetic analysis of affected individuals is lacking. Here we performed whole genome single-nucleotide polymorphism (SNP)...

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Source

Identifiers

PMID: 29923248
DOI: 10.1111/jsr.12718

Genes

LMOD3

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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