Volume 77, Issue 5, Pages (March 2010)

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Presentation transcript:

Volume 77, Issue 5, Pages 383-385 (March 2010) Evidence of true genotype–phenotype correlation in primary hyperoxaluria type 1 Bernd Hoppe Kidney International Volume 77, Issue 5, Pages 383-385 (March 2010) DOI: 10.1038/ki.2009.471 Copyright © 2010 International Society of Nephrology Terms and Conditions

Figure 1 Glyoxylate metabolism in patients with primary hyperoxaluria type I and II. X expresses block by enzymatic defect in case of primary hyperoxaluria type I (alanine:glyoxylate-aminotransferase (AGT); red) and in case of primary hyperoxaluria type II (glycolate-reductase/d-glycerate-dehydrogenase (GR), hydroxypyruvate-reductase (HPR); blue). Glycolate-oxidase (GO), d-amino-oxidase (DAO), lactate-dehydrogenase (LDH), glutamate:glyoxylate-aminotransferase (GGT), hydroxypyruvate-decarboxylase (HPDC), aldehyde-dehydrogenase (ADH), glycolate-dehydrogenase (GDH), d-glycerate dehydrogenase (DGDH). Kidney International 2010 77, 383-385DOI: (10.1038/ki.2009.471) Copyright © 2010 International Society of Nephrology Terms and Conditions