ENZYMOLOGICAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1 BY MEASUREMENT OF HEPATIC ALANINE: GLYOXYLATE AMINOTRANSFERASE ACTIVITY
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference28 articles.
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2. The metabolic defect of primary hyperoxaluria;Smith;Trans Assoc Am Physicians,1964
3. The metabolic error in primary hyperoxaluria;Hockaday;Arch Dis Child,1965
4. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I;Danpure;FEBS Lett,1986
5. Peroxisomal localization of alanine:glyoxylate aminotransferase in human liver;Noguchi;Arch Biochem Biophys,1979
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