Full text
PDF


Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Eldjarn L., Jellum E., Stokke O., Pande H., Waaler P. E. Beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria: a new inborn error of metabolism. Lancet. 1970 Sep 5;2(7671):521–522. doi: 10.1016/s0140-6736(70)90140-6. [DOI] [PubMed] [Google Scholar]
- Gompertz D., Draffan G. H. The gas-chromatographic diagnosis of intermittent maple syrup urine disease (branch-chain ketoaciduria). Clin Chim Acta. 1972 Aug;40(1):5–11. doi: 10.1016/0009-8981(72)90244-6. [DOI] [PubMed] [Google Scholar]
- Gompertz D., Draffan G. H. The identification of tiglylglycine in the urine of a child with -methylcrotonylglycinuria. Clin Chim Acta. 1972 Mar;37:405–410. doi: 10.1016/0009-8981(72)90462-7. [DOI] [PubMed] [Google Scholar]
- Gompertz D., Draffan G. H., Watts J. L., Hull D. Biotin-responsive beta-methylcrotonylglycinuria. Lancet. 1971 Jul 3;2(7714):22–24. doi: 10.1016/s0140-6736(71)90009-2. [DOI] [PubMed] [Google Scholar]
- Stokke O., Eldjarn L., Jellum E., Pande H., Waaler P. E. Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation. Pediatrics. 1972 May;49(5):726–735. [PubMed] [Google Scholar]