Subject
Nephrology,Genetics,Physiology,General Medicine
Reference25 articles.
1. Danpure CJ: Primary Hyperoxaluria; in Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (eds): The Molecular and Metabolic Bases of Inherited Disease. New York, McGraw-Hill, 2001, vol II, pp 3323-3367.
2. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I
3. Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.
4. An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.
Cited by
64 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献