Different Organic Acid Patterns in Urine and in Cerebrospinal Fluid in a Patient with Biotinidase Deficiency
- 1 January 1984
- book chapter
- Published by Springer Nature in Journal of Inherited Metabolic Disease
Abstract
No abstract availableKeywords
This publication has 2 references indexed in Scilit:
- Two forms of biotin‐responsive multiple carboxylase deficiencyJournal of Inherited Metabolic Disease, 1981
- Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: A biotin‐responsive disorderAnnals of Neurology, 1980