A familial study of a human enzyme defect, argininosuccinic aciduria
- 14 January 1964
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 14 (4) , 307-312
- https://doi.org/10.1016/s0006-291x(64)80001-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern IrelandArchives of Disease in Childhood, 1962
- Argininosuccinic Aciduria: An Inborn Error of Amino Acid MetabolismArchives of Disease in Childhood, 1961
- Determination of Argininosuccinic Acid by Ion-Exchange ChromatographyNature, 1961
- Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studiesBiochemical Journal, 1960
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960
- Renal clearances of amino acids in normal adults and in patients with aminoaciduriaBiochemical Journal, 1960
- Automatic Recording Apparatus for Use in Chromatography of Amino AcidsAnalytical Chemistry, 1958
- A DISEASE, PROBABLY HEREDITARY, CHARACTERISED BY SEVERE MENTAL DEFICIENCY AND A CONSTANT GROSS ABNORMALITY OF AMINOACID METABOLISMThe Lancet, 1958
- BIOSYNTHESIS OF UREAPublished by Elsevier ,1953