Isolated (biotin‐resistant) 3‐methylcrotonyl‐CoA carboxylase deficiency presenting at age 20 months with sopor, hypoglycaemia and ketoacidosis
- 1 June 1987
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 10 (S2), 290-292
- https://doi.org/10.1007/bf01811429
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sampleClinica Chimica Acta; International Journal of Clinical Chemistry, 1985
- 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