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BioMed Research International
Volume 2013 (2013), Article ID 687658, 15 pages
http://dx.doi.org/10.1155/2013/687658
Review Article

Protein Homeostasis Defects of Alanine-Glyoxylate Aminotransferase: New Therapeutic Strategies in Primary Hyperoxaluria Type I

1Departamento de Química-Física, Facultad de Ciencias, Universidad de Granada, Avenida Fuentenueva s/n, 18071 Granada, Spain
2Departamento de Cristalografía y Biología Estructural, Instituto de Química Física “Rocasolano”, Consejo Superior de Investigaciones Científicas, Serrano 119, 28006 Madrid, Spain
3Centre for Biomedical Research on Rare Diseases (CIBERER), University Hospital of the Canary Islands, and CIBICAN, University of La Laguna, 38320 Tenerife, Spain

Received 28 April 2013; Accepted 23 May 2013

Academic Editor: Barbara Cellini

Copyright © 2013 Angel L. Pey et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [1 citation]

The following is the list of published articles that have cited the current article.

  • Barbara Cellini, Riccardo Montioli, Elisa Oppici, Alessandra Astegno, and Carla Borri Voltattorni, “The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes,” Clinical Biochemistry, 2013. View at Publisher · View at Google Scholar