| Literature DB >> 30851244 |
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.Entities:
Keywords: De novo mutations; Epileptic encephalopathies; GABA(A) receptors; GABR genes; Genetic epilepsy syndromes; Missense mutations
Mesh:
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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