The enzyme defect in maple syrup urine disease (branched chain ketoaciduria).
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[1] J. Dancis,et al. DETECTION OF THE HETEROZYGOTE IN MAPLE SYRUP URINE DISEASE. , 1965, The Journal of pediatrics.
[2] J. Neel,et al. GENETIC HETEROGENEITY IN HUMAN ACATALASIA. , 1963, American journal of human genetics.
[3] M. Ehrlich,et al. [ANOTHER HETEROZYGOTE TEST FOR THE MAPLE SYRUP URINE DISEASE]. , 1963, Klinische Wochenschrift.
[4] R. Westall. Dietary Treatment of a Child with Maple Syrup Urine Disease (Branched-chain Ketoaciduria) , 1963, Archives of disease in childhood.
[5] J. Dancis,et al. THE DIAGNOSIS OF MAPLE SYRUP URINE DISEASE (BRANCHED- CHAIN KETOACIDURIA) BY THE IN VITRO STUDY OF THE PERIPHERAL LEUKOCYTE. , 1963, Pediatrics.
[6] M. Ehrlich,et al. Heterozygoten-Test fr die Ahornsirupkrankheit: Maple Syrup Urine Disease , 1963 .
[7] J. Dancis,et al. THE METABOLISM OF LEUCINE IN TISSUE CULTURE OF SKIN FIBROBLASTS OF MAPLE-SYRUP-URINE DISEASE. , 1963, Biochimica et biophysica acta.
[8] D. Burk,et al. Leukocyte preparations from human blood: evaluation of their morphologic and metabolic state. , 1962, The Journal of laboratory and clinical medicine.
[9] J. Dancis,et al. Metabolism of the white blood cells in maple-syrup-urine disease. , 1960, Biochimica et biophysica acta.
[10] A. D. Patrick. Maple Syrup Urine Disease , 1961, Archives of disease in childhood.
[11] J. Menkes. Maple syrup disease; isolation and identification of organic acids in the urine. , 1959, Pediatrics.
[12] J. Dancis,et al. “Maple Syrup Urine Disease” , 1959, British medical journal.
[13] J. Craig,et al. A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. , 1954, Pediatrics.
[14] D. E. Green,et al. l-Amino acid oxidase of animal tissue. , 1944 .