Cystinuria: biochemical evidence for three genetically distinct diseases.
Open Access
- 1 March 1966
- journal article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 45 (3) , 365-371
- https://doi.org/10.1172/jci105351
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- A MICROCOLORIMETRIC DETERMINATION OF CREATINE IN URINE BY THE JAFFE REACTIONPublished by Elsevier ,2021
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- Defective Uptake of Basic Amino Acids and l-Cystine by Intestinal Mucosa of Patients with Cystinuria *Journal of Clinical Investigation, 1964
- Evidence against a Single Renal Transport Defect in CystinuriaNew England Journal of Medicine, 1964
- Cystinuria: In vitro Demonstration of an Intestinal Transport DefectScience, 1964
- Studies of the kinetics of amino acid transport, incorporation into protein and oxidation in kidney-cortex slicesBiochimica et Biophysica Acta, 1963
- The intestinal absorption defect in cystinuriaGut, 1961
- THE CONCENTRATIONS OF CYSTEINE AND CYSTINE IN HUMAN BLOOD PLASMAJournal of Clinical Investigation, 1960
- PHENOTYPES AND GENOTYPES IN CYSTINURIAAnnals of Human Genetics, 1955
- THE PATTERN OF AMINO‐ACID EXCRETION IN CYSTINURIAAnnals of Human Genetics, 1955