Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolism
- 1 October 1982
- journal article
- research article
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 101 (4), 551-554
- https://doi.org/10.1016/s0022-3476(82)80698-7
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Gas chromatography of urinary N-phenylacetylglutamineJournal of Chromatography B: Biomedical Sciences and Applications, 1979
- Studies on a child suspected of having a deficiency in 3-hydroxy-3-methylglutaryl-CoA lyaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-Coa lyase deficiency: Facts and artefactsClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- 3-Methylglutaconic aciduria: Report on a sibship with infantile progressive encephalopathyEuropean Journal of Pediatrics, 1978
- Metabolic Studies of a Family with Massive Formiminoglutamic AciduriaPediatric Research, 1975
- Speech and Histidinemia: Methodology and Evaluation of Four CasesDevelopmental Medicine and Child Neurology, 1970