Possibility of inborn defect in isovalericacidaemia involving altered enzyme specificity rather than total inactivity
- 1 March 1974
- journal article
- Published by Springer Nature in Nature
- Vol. 248 (5444), 140-142
- https://doi.org/10.1038/248140a0
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Isovaleric acidemia: Identification of isovalerate, isovalerylglycine, and 3-hydroxyisovalerate in urine of a patient previously reported as having butyric and hexanoic acidemiaThe Journal of Pediatrics, 1973
- Isovaleric and α-Methylbutyric Acidemias Induced by Hypoglycin A: Mechanism of Jamaican Vomiting SicknessScience, 1972
- Studies of the mechanism of the hypoglycemic action of 4-pentenoic acid.Proceedings of the National Academy of Sciences, 1967
- Inhibition of the oxidation of leucine by hypoglycinBiochimica et Biophysica Acta (BBA) - General Subjects, 1967
- An inborn error of short-chain fatty acid metabolismThe Journal of Pediatrics, 1967
- Metabolic effects of hypoglycin and methylenecyclopropaneacetic acidBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1966
- Isovaleric acidemia: a new genetic defect of leucine metabolism.Proceedings of the National Academy of Sciences, 1966
- Idiopathic Hypervalinemia: Valine and Alpha Keto-acids in Blood Following an Oral Dose of ValineThe Tohoku Journal of Experimental Medicine, 1965
- Metabolism and metabolic effects of hypoglycinBiochimica et Biophysica Acta (BBA) - General Subjects, 1964
- Hypoglycin A,B: Biologically Active Polypeptides from Blighia sapidaNature, 1954