1. Kalkan, Zeynep, Durasi, İlknur Melis, Sezerman, Ugur, Atasever-Arslan, Belkis. 2016. Potential of GRID2 receptor gene for preventing TNF-induced neurodegeneration in autism. In Neuroscience letters, 620, 62-9. doi:10.1016/j.neulet.2016.03.043. https://pubmed.ncbi.nlm.nih.gov/27019035/
2. Hao, Shijie, Zhu, Xiaojia, Huang, Zhi, Sun, Yidi, Liu, Cirong. 2024. Cross-species single-cell spatial transcriptomic atlases of the cerebellar cortex. In Science (New York, N.Y.), 385, eado3927. doi:10.1126/science.ado3927. https://pubmed.ncbi.nlm.nih.gov/39325889/
3. Moura, Ronald, Tricarico, Paola Maura, Campos Coelho, Antonio Victor, Crovella, Sergio. 2014. GRID2 a novel gene possibly associated with mevalonate kinase deficiency. In Rheumatology international, 35, 657-9. doi:10.1007/s00296-014-3115-y. https://pubmed.ncbi.nlm.nih.gov/25146332/
4. Huang, Shengzhu, Zhang, Chenqi, Xie, Xing, Ye, Li, Hu, Yanling. 2022. GRID2 aberration leads to disturbance in neuroactive ligand-receptor interactions via changes to the species richness and composition of gut microbes. In Biochemical and biophysical research communications, 631, 9-17. doi:10.1016/j.bbrc.2022.09.006. https://pubmed.ncbi.nlm.nih.gov/36162328/
5. Panda, Prateek Kumar, Sharawat, Indar Kumar, Dawman, Lesa. 2020. GRID2 Mutation-Related Spinocerebellar Ataxia Type 18: A New Report and Literature Review. In Journal of pediatric genetics, 11, 99-109. doi:10.1055/s-0040-1721084. https://pubmed.ncbi.nlm.nih.gov/35769960/
6. Coutelier, Marie, Burglen, Lydie, Mundwiller, Emeline, Stevanin, Giovanni, Durr, Alexandra. 2015. GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia. In Neurology, 84, 1751-9. doi:10.1212/WNL.0000000000001524. https://pubmed.ncbi.nlm.nih.gov/25841024/
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