Varaico: Literature-Extracted Genetic Variants

Gene:GABRB3
Variant:p.L170R
Back to variants list

GABRB3

NM_000814.6:p.L170R

Associated Papers

Clinical and functional characterization of the GABRB3 p.Met80Val variant in early-onset epilepsy with long-term follow-up.

Hua R et al.

Italian Journal of Pediatrics, 2025

Identification and Classification of Position-specific GABAA Receptor Subunit Missense Variants for Their Role In Hippocampal Pyramidal Neurons.

Arslan A et al.

Journal of Visualized Experiments : Jove, 2025

40549733 (PubMed )
Supplement: R_Supplementary20File204_11_May_2025.zip › R_Supplementary_File_4_11_May_2025 › Supplementary_Table_S16.xlsx › Suppl_Table_S16

GABAA receptors in epilepsy: Elucidating phenotypic divergence through functional analysis of genetic variants.

Absalom NL et al.

Journal of Neurochemistry, 2024

GABA(A) Receptor Subunit (γ2, δ, β1-3) Variants in Genetic Epilepsy: A Comprehensive Summary of 206 Clinical Cases.

Zhu X et al.

Journal of Child Neurology, 2024

Correlations of receptor desensitization of gain-of-function GABRB3 variants with clinical severity.

Lin SXN et al.

Brain : a Journal of Neurology, 2024

Pathogenicity Prediction of GABAA Receptor Missense Variants.

Wang YJ et al.

Biorxiv : the Preprint Server for Biology, 2023

Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype-phenotype correlation.

Maillard PY et al.

Epilepsia, 2022

35718920 (PubMed )
Supplement: EPI-63-2519-s001.xlsx › Feuil1

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.

Yang Y et al.

Journal of Neurology, 2022

Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies.

Absalom NL et al.

Nature Communications, 2022

Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes.

Shi YW et al.

Brain : a Journal of Neurology, 2019

GABA A Receptor Coupling Junction and Pore GABRB3 Mutations are Linked to Early-Onset Epileptic Encephalopathy.

Hernandez CC et al.

Scientific Reports, 2017

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."