Clinical and laboratory observationPrimary oxaluria type 2 (l-glyceric aciduria): A rare cause of nephrolithiasis in children
References (10)
- et al.
Evidence for a mammalian d-glycerate dehydrogenase
J Biol Chem
(1962) - et al.
l-Glyceric aciduria: a new genetic variant of primary hyperoxaluria
N Engl J Med
(1968) - et al.
l-Glyceric aciduria (primary hyperoxaluria type 2) in siblings in two unrelated families
J Inherited Metab Dis
(1984) - et al.
Hepatic d-glycerate dehydrogenase and glyoxylate reductase deficiency in primary hyperoxaluria type 2
Biochem Soc Trans
(1988) - et al.
The oxidation of d- and l-glycerate by rat liver
Biochem J
(1965)
There are more references available in the full text version of this article.
Cited by (0)
Copyright © 1991 Published by Mosby, Inc.