Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria.

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Published in J Clin Invest on December 01, 2010

Authors

Charles G Bailey1, Renae M Ryan, Annora D Thoeng, Cynthia Ng, Kara King, Jessica M Vanslambrouck, Christiane Auray-Blais, Robert J Vandenberg, Stefan Bröer, John E J Rasko

Author Affiliations

1: Gene and Stem Cell Therapy Program, Centenary Institute, Camperdown, New South Wales, Australia.

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