Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria. | J Clin Invest;121(1): 446-53, 2011 Jan. | MEDLINE

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

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

Affiliation

Bailey CG; Gene and Stem Cell Therapy Program, Centenary Institute, Camperdown, New South Wales, Australia.

J Clin Invest ; 121(1): 446-53, 2011 Jan.

Article in En | MEDLINE | ID: mdl-21123949

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Excitatory Amino Acid Transporter 3 / Mutation Type of study: Prognostic_studies Language: En Journal: J Clin Invest Year: 2011 Document type: Article Affiliation country: Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Excitatory Amino Acid Transporter 3 / Mutation Type of study: Prognostic_studies Language: En Journal: J Clin Invest Year: 2011 Document type: Article Affiliation country: Country of publication: