BIOTINIDASE DEFICIENCY IN JUVENILE MULTIPLE CARBOXYLASE DEFICIENCY
- 1 August 1983
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 322 (8346), 398
- https://doi.org/10.1016/s0140-6736(83)90364-1
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Phenotypic variation in biotinidase deficiencyThe Journal of Pediatrics, 1983
- Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- Impaired Intestinal Absorption of Biotin in Juvenile Multiple Carboxylase DeficiencyNew England Journal of Medicine, 1983
- Deficient Biotinidase Activity in Late-Onset Multiple Carboxylase DeficiencyNew England Journal of Medicine, 1983
- A simple method for determination of plasma and urinary biotinClinica Chimica Acta; International Journal of Clinical Chemistry, 1982
- Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.JCI Insight, 1981
- DEFECTIVE BIOTIN ABSORPTION IN MULTIPLE CARBOXYLASE DEFICIENCYThe Lancet, 1981
- Biotin-Responsive Carboxylase Deficiency Associated with Subnormal Plasma and Urinary BiotinNew England Journal of Medicine, 1981
- DiscussionThe American Journal of Clinical Nutrition, 1967
- Incidence and Significance of Hypovitaminemia in a Randomly Selected Municipal Hospital PopulationThe American Journal of Clinical Nutrition, 1965