Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology
- 1 September 1995
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 18 (5) , 643-645
- https://doi.org/10.1007/bf02436014
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Standardized method for high-resolution 1H-NMR of cerebrospinal fluidClinical Chemistry, 1995
- Cerebrospinal fluid organic acids in biotinidase deficiencyJournal of Inherited Metabolic Disease, 1993
- Intercurrent illness in inborn errors of intermediary metabolism.Archives of Disease in Childhood, 1992