LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference16 articles.
1. Familial temporal lobe epilepsy: A common disorder identified in twins
2. Localization of a gene for partial epilepsy to chromosome 10q
3. Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q
4. Autosomal dominant partial epilepsy with auditory features: Defining the phenotype
5. Supporting evidence of a gene for partial epilepsy on 10q
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1. Clinical Correlation of Altered Molecular Signatures in Epileptic Human Hippocampus and Amygdala;Molecular Neurobiology;2023-09-02
2. A patient-derived mutation of epilepsy-linked LGI1 increases seizure susceptibility through regulating Kv1.1;Cell & Bioscience;2023-02-20
3. Limbic Encephalitis and Autoimmune Encephalitides: Pathophysiology, Classification, Clinical Presentation, and Treatment;World Journal of Neuroscience;2023
4. Autosomal dominant lateral temporal epilepsy in a family exhibiting a rare heterozygous mutation and deletion in the leucine-rich glioma inactivated 1 gene;Neuroscience Letters;2022-06
5. Ictal aphasia in LGI1-related autosomal dominant epilepsy with auditory features;Practical Neurology;2022-03-30
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