Isolated biotin‐resistant 3‐methylcrotonyl‐CoA carboxylase deficiency presenting as a Reye syndrome‐like illness
- 1 September 1989
- journal article
- research article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 12 (3), 339-340
- https://doi.org/10.1007/bf01799234
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Isolated (biotin‐resistant) 3‐methylcrotonyl‐CoA carboxylase deficiency presenting at age 20 months with sopor, hypoglycaemia and ketoacidosisJournal of Inherited Metabolic Disease, 1987
- Isolated biotin‐resistant 3‐methylcrotonyl CoA carboxylase deficiency presenting with life‐threatening hypoglycaemiaJournal of Inherited Metabolic Disease, 1984
- Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibsEuropean Journal of Pediatrics, 1982
- Evidence for the enzymic defect in β‐methylcrotonylglycinuriaFEBS Letters, 1973