Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria-Reference-Cited by-同舟云学术

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

Published:2011-01-04 Issue:1 Volume:121 Page:446-453
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

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.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference45 articles.

1. Quebec neonatal mass urinary screening programme: From micromolecules to macromolecules

2. Dicarboxylic aminoaciduria: An inborn error of glutamate and aspartate transport with metabolic implications, in combination with a hyperprolinemia

3. Dicarboxylic aminoaciduria associated with mental retardation

4. Primary structure and functional characterization of a high-affinity glutamate transporter

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