Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria.
Bailey CG; Ryan RM; Thoeng AD; Ng C; King K; Vanslambrouck JM; Auray-Blais C; Vandenberg RJ; Bröer S; Rasko JE; The Journal Of Clinical Investigation, 2011, vol. 121, issue 1, p 446, ISSN 15588238. ISBN 15588238.

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