Enzyme defect in skin fibroblasts in intermittent branched-chain detonuria and in maple syrup urine disease
- 30 April 1969
- journal article
- Published by Elsevier in Biochemical Medicine
- Vol. 2 (5), 407-411
- https://doi.org/10.1016/0006-2944(69)90043-x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
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- Branched Chain α-Keto Acid MetabolismPublished by Elsevier ,1968
- Isovaleric AcidemiaNew England Journal of Medicine, 1967
- Biochemical studies on branched-chain oxoacid oxidasesBiochimica et Biophysica Acta (BBA) - Enzymology, 1967
- Intermittent Branched-Chain KetonuriaNew England Journal of Medicine, 1967
- Late Manifesting Variant of Branched-Chain Ketoaciduria (Maple Syrup Urine Disease)Acta Paediatrica, 1964
- The metabolism of leucine in tissue culture of skin fibroblasts of maple-syrup-urine diseaseBiochimica et Biophysica Acta, 1963
- Maple Syrup Urine DiseaseAmerican Journal of Diseases of Children, 1963
- Maple syrup diseaseNeurology, 1959
- "Maple Syrup Urine Disease"BMJ, 1959