1. Martinez-Esteve Melnikova, Anastasia, Pijuan, Jordi, Aparicio, Javier, Hoenicka, Janet, San Antonio-Arce, Victoria. 2022. The p.Glu787Lys variant in the GRIA3 gene causes developmental and epileptic encephalopathy mimicking structural epilepsy in a female patient. In European journal of medical genetics, 65, 104442. doi:10.1016/j.ejmg.2022.104442. https://pubmed.ncbi.nlm.nih.gov/35093607/
2. Maher, Bridget H, Lea, Rod A, Follett, Jordan, Haupt, Larisa M, Griffiths, Lyn R. 2013. Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort. In Headache, 53, 1245-9. doi:10.1111/head.12151. https://pubmed.ncbi.nlm.nih.gov/23772601/
3. Singh, Tarjinder, Poterba, Timothy, Curtis, David, Neale, Benjamin M, Daly, Mark J. 2022. Rare coding variants in ten genes confer substantial risk for schizophrenia. In Nature, 604, 509-516. doi:10.1038/s41586-022-04556-w. https://pubmed.ncbi.nlm.nih.gov/35396579/
4. Rinaldi, Berardo, Ge, Yu-Han, Freri, Elena, Marchisio, Paola, Milani, Donatella. 2021. Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene. In Neurogenetics, 23, 27-35. doi:10.1007/s10048-021-00666-1. https://pubmed.ncbi.nlm.nih.gov/34731330/