Urea cycle disorders—update
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/s10038-019-0614-4.pdf
Reference74 articles.
1. Schutz Y. Protein turnover, ureagenesis and gluconeogenesis. Int J Vitam Nutr Res. 2011;81:101–7.
2. Haberle J, Gorg B, Rutsch F, et al. Congenital glutamine deficiency with glutamine synthetase mutations. N Engl J Med. 2005;353:1926–33.
3. James LA, Lunn PG, Middleton S and Elia M. Distribution of glutaminase and glutamine synthetase activities in the human gastrointestinal tract. Clin Sci. 1998;94:313–9.
4. Levitt DG and Levitt MD. Gastrointestinal urease in man. I Activity of mucosal urease. Gut. 1966;7:631–5.
5. Levitt DG, Levitt MD. A model of blood-ammonia homeostasis based on a quantitative analysis of nitrogen metabolism in the multiple organs involved in the production, catabolism, and excretion of ammonia in humans. Clin Exp Gastroenterol. 2018;11:193–215.
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