Pyruvate carboxylase responsive to ketosis in a multiple carboxylase deficiency patient
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF01799735
Reference9 articles.
1. Atkin, B. M., Utter, M. F. and Weinberg, M. B. Pyruvate carboxylase and phosphoenolpyruvate carboxykinase activity in leukocytes and fibroblasts from a patient with pyruvate carboxylase deficiency.Pediatr. Res. 13 (1979) 38–43
2. Bartlett, K., Ghneim, H. K., Stirk, J. H., Dale, G. and Alberti, G. M. M. Pyruvate carboxylase deficiency.J. Inher. Metab. Dis. 7, Suppl. 1 (1984) 74–78
3. Cazzulo, J. J., Claisse, L. M. and Stoppani, O. M. Carboxylase levels and carbon dioxide fixation in bakers' yeast.J. Bact. 96 (1968) 623–628
4. Cazzulo, J. J., Sundaram, T. K. and Kornberg, H. L. Properties and regulation of pyruvate carboxylase fromBacillus stearonthermophilus.Proc. Roy. Soc. London B 176 (1970) 1–19
5. Chang, H. I. and Cohen, N. D. Regulation and intracellular localization of the biotin holocarboxylase synthetase of 3T3-L1 cellsArch. Biochem. Biophys. 225 (1983) 237–247
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