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

2011

Field of Research

  • Receptors And Membrane Biology

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