Iminoaciduria: A benign renal tubular defect
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference15 articles.
1. Renal tubular dysfunction;Woolf,1966
2. Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness;Schafer;New Eng. J. Med.,1962
3. Amino acid transport: Evidence for genetic control of two types in human kidney;Scriver;Science,1967
4. Glycinurie et iminoacidurie fenale associées à une oligophrénie, Etude clinique et biochimique;Mardens;J. Neurol. Sci.,1968
5. Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids;Tancredi;J. Pediat.,1970
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