| 1 | MRT48, SLC6A17 |
| Homozygous SLC6A17 Mutations Cause Autosomal-Recessive Intellectual Disability with Progressive Tremor, Speech Impairment, and Behavioral Problems. | |
| Iqbal Z, Willemsen MH, Papon MA, Musante L, Benevento M, Hu H, Venselaar H, Wissink-Lindhout WM, Vulto-van Silfhout AT, Vissers LE, de Brouwer AP, Marouillat S, Wienker TF, Ropers HH, Kahrizi K, Nadif Kasri N, Najmabadi H, Laumonnier F, Kleefstra T, van Bokhoven H. | |
| Am J Hum Genet 96(3):386-96. doi: 10.1016/j.ajhg.2015.01.010. Epub 2015 Feb 19. 2015 | |
| 2 | SLC6A17 |
| Synaptic Vesicle Protein NTT4/XT1 (SLC6A17) Catalyzes Na+-coupled Neutral Amino Acid Transport. | |
| Zaia KA, Reimer RJ. | |
| J Biol Chem 284(13):8439-48. Epub 2009 Jan 15. 2009 | |
| 3 | SLC6A17, SLC6A18 |
| The repertoire of solute carriers of family 6: identification of new human and rodent genes. | |
| Höglund PJ, Adzic D, Scicluna SJ, Lindblom J, Fredriksson R. | |
| Biochem Biophys Res Commun 336(1):175-89. 2005 | |