1. Bhumika, S, Basalingappa, Kanthesh M, Gopenath, T S, Basavaraju, Suman. 2022. Glycine encephalopathy. In The Egyptian journal of neurology, psychiatry and neurosurgery, 58, 132. doi:10.1186/s41983-022-00567-6. https://pubmed.ncbi.nlm.nih.gov/36415754/
2. Curtis, David. . Do damaging variants of SLC6A9, the gene for the glycine transporter 1 (GlyT-1), protect against schizophrenia? In Psychiatric genetics, 30, 150-152. doi:10.1097/YPG.0000000000000260. https://pubmed.ncbi.nlm.nih.gov/32796235/
3. Ueno, Takahiro, Tabara, Yasuharu, Fukuda, Noboru, Miki, Tetsuro, Soma, Masayoshi. 2009. Association of SLC6A9 gene variants with human essential hypertension. In Journal of atherosclerosis and thrombosis, 16, 201-6. doi:. https://pubmed.ncbi.nlm.nih.gov/19556729/
4. Tscherner, Allison K, McClatchie, Taylor, Kaboba, Gracia, Boison, Detlev, Baltz, Jay M. 2023. Oocyte-Specific Deletion of Slc6a9 Encoding the GLYT1 Glycine Transporter Eliminates Glycine Transport in Mouse Preimplantation Embryos and Their Ability to Counter Hypertonic Stress. In Cells, 12, . doi:10.3390/cells12202500. https://pubmed.ncbi.nlm.nih.gov/37887344/
5. Docherty, Anna R, Mullins, Niamh, Ashley-Koch, Allison E, Kimbrel, Nathan A, Ruderfer, Douglas M. . GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. In The American journal of psychiatry, 180, 723-738. doi:10.1176/appi.ajp.21121266. https://pubmed.ncbi.nlm.nih.gov/37777856/
6. Hauf, K, Barsch, L, Bauer, D, Grasshoff, U, Eulenburg, V. 2020. GlyT1 encephalopathy: Characterization of presumably disease causing GlyT1 mutations. In Neurochemistry international, 139, 104813. doi:10.1016/j.neuint.2020.104813. https://pubmed.ncbi.nlm.nih.gov/32712301/
7. Taylor, Danielle L, Tiwari, Arun K, Lieberman, Jeffrey A, Müller, Daniel J, Kennedy, James L. 2016. Pharmacogenetic Analysis of Functional Glutamate System Gene Variants and Clinical Response to Clozapine. In Molecular neuropsychiatry, 2, 185-197. doi:10.1159/000449224. https://pubmed.ncbi.nlm.nih.gov/28277565/
8. Alfadhel, Majid, Nashabat, Marwan, Qahtani, Hanan Al, Alkuraya, Fowzan, Ali, Qais Abu. 2016. Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans. In Human genetics, 135, 1263-1268. doi:. https://pubmed.ncbi.nlm.nih.gov/27481395/
智鼠故事 
