Diagnosis and Mutational Analysis of Maple Syrup Urine Disease Using Cell Cultures
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Elsevier
Reference24 articles.
1. Metabolism of the white blood cells in maple-syrup-urine disease
2. Metabolic and Molecular Bases of Inherited Disease;Chuang,1995
3. Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy
4. The metabolism of leucine in tissue culture of skin fibroblasts of maple-syrup-urine disease
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