3‐Methylglutaconic aciduria presenting as Reye syndrome in a Chinese boy
- 1 September 1995
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 18 (5) , 645-646
- https://doi.org/10.1007/bf02436015
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Multiple syndromes of 3-methylglutaconic aciduriaPediatric Neurology, 1993
- 3‐methylglutaconyl‐coenzyme‐A hydratase deficiency: A new caseJournal of Inherited Metabolic Disease, 1992
- 3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: A coupled enzyme assay useful for their detectionClinica Chimica Acta; International Journal of Clinical Chemistry, 1989