Scientific article
English

Towards the identification of a genetic basis for Landau-Kleffner syndrome

Published inEpilepsia, vol. 55, no. 6, p. 858-865
Publication date2014
Abstract

To establish the genetic basis of Landau-Kleffner syndrome (LKS) in a cohort of two discordant monozygotic (MZ) twin pairs and 11 isolated cases.

Keywords
  • Adolescent
  • Adult
  • Cell Adhesion Molecules/genetics
  • Cell Adhesion Molecules, Neuronal/genetics
  • Child
  • Comparative Genomic Hybridization
  • Extracellular Matrix Proteins/genetics
  • Female
  • Genetic Predisposition to Disease/genetics
  • Humans
  • Landau-Kleffner Syndrome/genetics
  • Male
  • Nerve Tissue Proteins/genetics
  • Oligonucleotide Array Sequence Analysis
  • Polymorphism, Single Nucleotide/genetics
  • Receptor, EphB2/genetics
  • Receptors, N-Methyl-D-Aspartate/genetics
  • Serine Endopeptidases/genetics
  • Twins, Monozygotic/genetics
  • Young Adult
Citation (ISO format)
CONROY, Judith et al. Towards the identification of a genetic basis for Landau-Kleffner syndrome. In: Epilepsia, 2014, vol. 55, n° 6, p. 858–865. doi: 10.1111/epi.12645
Main files (1)
Article (Published version)
accessLevelRestricted
Identifiers
Journal ISSN0013-9580
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