Biotin in Metabolism and Its Relationship to Human Disease
- 1 September 2002
- journal article
- review article
- Published by Elsevier in Archives of Medical Research
- Vol. 33 (5) , 439-447
- https://doi.org/10.1016/s0188-4409(02)00399-5
Abstract
No abstract availableKeywords
This publication has 84 references indexed in Scilit:
- Molecular Characterization of the Non-biotin-containing Subunit of 3-Methylcrotonyl-CoA CarboxylasePublished by Elsevier ,2000
- Marginal Biotin Deficiency Is TeratogenicProceedings of the Society for Experimental Biology and Medicine, 2000
- Conflicting indicators of biotin status from a cross-sectional study of normal pregnancy.Journal of the American College of Nutrition, 1997
- Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: The usefulness of multiple study designsAmerican Journal of Medical Genetics, 1993
- Clinical Findings in Four Children with Biotinidase Deficiency Detected through a Statewide Neonatal Screening ProgramNew England Journal of Medicine, 1985
- Biotinidase deficiency: A novel vitamin recycling defectJournal of Inherited Metabolic Disease, 1985
- Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onsetThe Journal of Pediatrics, 1982
- Organic aciduria in neonatal multiple carboxylase deficiencyJournal of Inherited Metabolic Disease, 1982
- The birA gene of Escherichia coli encodes a biotin holoenzyme synthetaseJournal of Molecular Biology, 1981
- Regulation of glycolysis in biotin-deficient rat liverLife Sciences, 1970