Alanine glyoxylate aminotransferase deficiency: Biochemical and molecular genetic lessons from the study of a human disease
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology,Molecular Medicine
Reference61 articles.
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3. Peroxisomal alanine: glyoxylate aminotransferase deficiency in primary hyperoxaluria type I;Danpure;FEBS Lett.,1986
4. Enzymological diagnosis of primary hyperoxaluria type I by measurement of hepatic alanine : glyoxylate aminotransferase activity;Danpure;Lancet,1987
5. l-glyceric aciduria: a new genetic variant of primary hyperoxaluria;Williams;N. Engl. J. Med.,1968
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