1. Matsumoto, Ken, Shimodaira, Masanori, Nakagawa, Tomoko, Sato, Naoyuki, Aoi, Noriko. 2011. Association study: SLC6A18 gene and myocardial infarction. In Clinical biochemistry, 44, 789-94. doi:10.1016/j.clinbiochem.2011.03.031. https://pubmed.ncbi.nlm.nih.gov/21420947/
2. Fargaly, Hithem, Mathew, Shobi, Rossi, Noreen F. 2022. Hyperglycinuria: diagnosis in middle age. In BMJ case reports, 15, . doi:10.1136/bcr-2021-246252. https://pubmed.ncbi.nlm.nih.gov/35236679/
3. Eslami, Bita, Kinboshi, Masato, Inoue, Sumiko, Inoue, Kayoko, Koizumi, Akio. . A nonsense polymorphism (Y319X) of the solute carrier family 6 member 18 (SLC6A18) gene is not associated with hypertension and blood pressure in Japanese. In The Tohoku journal of experimental medicine, 208, 25-31. doi:. https://pubmed.ncbi.nlm.nih.gov/16340170/
4. Wang, Weijing, Yao, Wenqin, Tan, Qihua, Xu, Chunsheng, Zhang, Dongfeng. 2023. Identification of key DNA methylation changes on fasting plasma glucose: a genome-wide DNA methylation analysis in Chinese monozygotic twins. In Diabetology & metabolic syndrome, 15, 159. doi:10.1186/s13098-023-01136-4. https://pubmed.ncbi.nlm.nih.gov/37461060/
5. Chhaya, Nisarg, Chan, Tineke. 2021. Retinopathy in a Full-Term Infant with Cri-du-Chat Syndrome. In Rhode Island medical journal (2013), 104, 37-39. doi:. https://pubmed.ncbi.nlm.nih.gov/33517598/