Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disorders
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799804
Reference4 articles.
1. Carson, N. A. J., Scally, B. G., Neill, D. W. and Carre, I. J. Saccharopinuria: a new inborn error of lysine metabolism.Nature 218 (1968) 679
2. Halperin, M. L., Schiller, C. M. and Fritz, I. B. The inhibition by methylmalonic acid of malate transport by the dicarboxylate carrier in rat liver mitochondria. A possible explanation for hypoglycemia in methylmalonic aciduria.J. Clin. Invest. 50 (1971) 2276–2280
3. Przyrembel, H., Wendel, U., Becker, K., Bremer, H. J., Bruinvis, L., Ketting, D. and Wadman, S. K. Glutaric aciduria type II: report on a previously undescribed metabolic disorder.Clin. Chim. Acta 66 (1976) 227–239
4. Sweetman, L., Nyhan, W. L., Trauner, D. A., Nerritt, T. A. and Singh, M. Glutaric aciduria type II.J. Pediatr. 96 (1980) 1020–1026
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3. Metabolic intermediates in lactic acidosis: compounds, samples and interpretation;Journal of Inherited Metabolic Disease;1996-07
4. Metabolism of citrulline in man;Amino Acids;1995
5. Lacticacidemia;Advances in Human Genetics;1989
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