Primary oxaluria type 2 (l-glyceric aciduria): A rare cause of nephrolithiasis in children
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. l-Glyceric aciduria: a new genetic variant of primary hyperoxaluria;Williams;N Engl J Med,1968
2. l-Glyceric aciduria (primary hyperoxaluria type 2) in siblings in two unrelated families;Chalmers;J Inherited Metab Dis,1984
3. Hepatic d-glycerate dehydrogenase and glyoxylate reductase deficiency in primary hyperoxaluria type 2;Mistry;Biochem Soc Trans,1988
4. Evidence for a mammalian d-glycerate dehydrogenase;Willis;J Biol Chem,1962
5. The oxidation of d- and l-glycerate by rat liver;Dawkins;Biochem J,1965
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