Literature DB >> 30851244

A structural look at GABAA receptor mutations linked to epilepsy syndromes.

Ciria C Hernandez1, Robert L Macdonald2.   

Abstract

Understanding the genetic variation in GABAA receptor subunit genes (GABRs), GABRA1-6, GABRB1-3, GABRG1-3 and GABRD, in individuals affected by epilepsy may improve the diagnosis and treatment of epilepsy syndromes through identification of disease-associated variants. However, the lack of functional analysis and validation of many novel and previously reported familial and de novo mutations have made it challenging to address meaningful gene associations with epilepsy syndromes. GABAA receptors belong to the Cys-loop receptor family. Even though GABAA receptor mutant residues are widespread among different GABRs, their frequent occurrence in important structural domains that share common functional features suggests associations between structure and function.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  De novo mutations; Epileptic encephalopathies; GABA(A) receptors; GABR genes; Genetic epilepsy syndromes; Missense mutations

Mesh:

Substances:

Year:  2019        PMID: 30851244     DOI: 10.1016/j.brainres.2019.03.004

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  23 in total

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