Treatment of hyperargininaemia due to arginase deficiency with a chemically defined diet
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800000
Reference18 articles.
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2. Benson, J. V., Jr., Gordon, M. J. and Patterson, J. A. Accelerated chromatographic analyses of amino acids in physiological fluids containing glutamine and asparagine.Anal. Biochem. 18 (1967) 228
3. Brusilow, S. W., Tinker, J. and Batshaw, M. L. Amino acid acylation: A mechanism of nitrogen excretion in inborn errors of urea synthesis.Science 207 (1980) 659
4. Cederbaum, S. D., Shaw, K. N. F. and Valente, M. Hyperargininemia.J. Pediatr. 90 (1977) 569
5. Cederbaum, S. D., Shaw, K. N. F., Spector, E. B., Snodgrass, P. J., Verity, M. A. and Sugarman, G. I. Hyperargininemia with arginase deficiency.Pediatr. Res. 13 (1979) 827
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