Clinical and biochemical findings on a child with multiple biotin‐responsive carboxylase deficiencies
- 1 June 1982
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 5 (2) , 67-68
- https://doi.org/10.1007/bf01799990
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Propionate Inhibition of Succinate: CoA Ligase (GDP) and the Citric Acid Cycle in MitochondriaPediatric Research, 1980
- Holocarboxylase synthetase deficiency: A biotin-responsive organic acidemiaThe Journal of Pediatrics, 1980
- Letter to the Editor: Measurement of Pyruvate Carboxylase Activity in Amniotic Fluid CellsPediatric Research, 1980
- Biotin-response OrganicaciduriaJournal of Clinical Investigation, 1979
- MULTIPLE BIOTIN-DEPENDENT CARBOXYLASE DEFICIENCIES ASSOCIATED WITH DEFECTS IN T-CELL AND B-CELL IMMUNITYThe Lancet, 1979
- Human Propionyl CoA Carboxylase: Some Properties of the Partially Purified Enzyme in Fibroblasts from Controls and Patients with Propionic AcidemiaPediatric Research, 1979
- BIOCHEMICAL DIFFERENCES BETWEEN MUTANT PROPIONYL-COA CARBOXYLASES FROM 2 COMPLEMENTATION GROUPS1978
- Propionyl-CoA Carboxylase Deficiency in a Patient with Biotin-responsive 3-MethylcrotonylglycinuriaPediatric Research, 1977