Disease: Autosomal dominant partial epilepsy with auditory features
- A de novo pathogenic variant in MICAL-1 causes epilepsy with auditory features
- A novel LGI1 missense mutation causes dysfunction in cortical neuronal migration and seizures
- A novel Lgi1 mutation causes white matter abnormalities and impairs motor coordination in mice
- A novel LGI1 mutation causing autosomal dominant lateral temporal lobe epilepsy confirmed by a precise knock-in mouse model
- ADAM22 and ADAM23 modulate the targeting of the Kv1 channel-associated protein LGI1 to the axon initial segment
- Autosomal Dominant Epilepsy with Auditory Features
- Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia
- Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation
- Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31
- Autosomal dominant temporal lobe epilepsy associated with heterozygous reelin mutation: 3 T brain MRI study with advanced neuroimaging methods
- Clinical characteristics and whole exon sequence study of a Chinese family with autosomal dominant lateral temporal lobe epilepsy
- CNTNAP2 mutations and autosomal dominant epilepsy with auditory features
- Down-Regulation of Astrocytic Kir4.1 Channels during the Audiogenic Epileptogenesis in <em>Leucine-Rich Glioma-Inactivated 1</em> (<em>Lgi1</em>) Mutant Rats
- Epilepsy with auditory features: Contribution of known genes in 112 patients
- EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities
- Genetic models of focal epilepsies
- Genetics advances in autosomal dominant focal epilepsies: focus on DEPDC5
- Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1/epitempin gene
- Imbalance of glutamatergic and GABAergic neurotransmission in audiogenic seizure-susceptible L<em>eucine-rich glioma-inactivated 1</em> (<em>Lgi1</em>)-mutant rats
- Insights into the mechanisms of epilepsy from structural biology of LGI1-ADAM22
- Leucine-Rich Glioma Inactivated 1 Promotes Oligodendrocyte Differentiation and Myelination via TSC-mTOR Signaling
- LGI proteins in the nervous system
- Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations
- Patient-derived antibodies reveal the subcellular distribution and heterogeneous interactome of LGI1
- Rescue of Normal Excitability in LGI1-Deficient Epileptic Neurons
- SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus
- Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation
- The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations
- The downregulation of Kv<sub>1</sub> channels in Lgi1<sup>-/-</sup>mice is accompanied by a profound modification of its interactome and a parallel decrease in Kv<sub>2</sub> channels
- The LGI1 protein: molecular structure, physiological functions and disruption-related seizures
- The Nogo Receptor Ligand LGI1 Regulates Synapse Number and Synaptic Activity in Hippocampal and Cortical Neurons