Congenital lysinuria: A new inherited transport disorder of dibasic amino acids
- 31 August 1970
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 77 (2), 259-266
- https://doi.org/10.1016/s0022-3476(70)80333-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Hyperdibasicaminoaciduria: An Inherited Disorder of Amino Acid Transport[34]Pediatric Research, 1968
- Enzymes of Urea Synthesis in Familial Protein Intolerance with Deficient Transport of Basic Amino AcidsActa Paediatrica, 1967
- Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 PatientsActa Paediatrica, 1967
- Cystinuria: Genetic Heterogeneity and AllelismScience, 1966
- Cystinuria: biochemical evidence for three genetically distinct diseases.Journal of Clinical Investigation, 1966
- PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINOACIDSThe Lancet, 1965
- Hyperlysinemia Associated with RetardationNew England Journal of Medicine, 1965
- Homocitrulline and Homoarginine Synthesis from LysineScience, 1964
- Natural occurrence of homocitrullineArchives of Biochemistry and Biophysics, 1962
- Automatic Recording Apparatus for Use in Chromatography of Amino AcidsAnalytical Chemistry, 1958