Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria
Citation
Bailey, C, Ryan, R, Thoeng, A et al 2011, 'Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria', Journal of Clinical Investigation, vol. 121, no. 1, pp. 446-453.Year
2011ANU Authors
Field of Research
- Receptors And Membrane Biology