Lysinuric protein intolerance, an autosomal recessive disease
- 1 July 1971
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 2 (4) , 214-222
- https://doi.org/10.1111/j.1399-0004.1971.tb00280.x
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
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- Congenital lysinuria: A new inherited transport disorder of dibasic amino acidsThe Journal of Pediatrics, 1970
- LEUCOCYTE GLUTAMINASE IN FAMILIAL PROTEIN INTOLERANCEThe Lancet, 1970
- Ornithine-ketoacid aminotransferase in human liver with reference to patients with hyperornithinaemia and familial protein intoleranceClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- Hyperdibasicaminoaciduria: An Inherited Disorder of Amino Acid Transport[34]Pediatric Research, 1968
- FAMILIAL PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINO ACIDSActa Medica Scandinavica, 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
- PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINOACIDSThe Lancet, 1965
- URINARY AMINO‐ACIDS IN MICE OF DIFFERENT GENOTYPESAnnals of Eugenics, 1953