Author:
Nakamura Kimitoshi,Kido Jun,Matsumoto Shirou,Mitsubuchi Hiroshi,Endo Fumio
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference19 articles.
1. Brusilow, S. W. & Horwich, A. L. in The Metabolic and Molecular Bases of Inherited Disease 8th edn (eds Scriver, C. R., Beaudet, A. L., Sly, W. S. & Valle, D.) 1909 (McGraw-Hill, New York, NY, USA, 2001).
2. Matsuda, I. & Tanase, S. The ornithine transcarbamylase (OTC) gene: mutations in 50 Japanese families with OTC deficiency. Am. J. Med. Genet. 71, 378–383 (1997).
3. Brusilow, S. W., Valle, D. L. & Batshaw, M. New pathways of nitrogen excretion in inborn errors of urea synthesis. Lancet 2, 452–454 (1979).
4. Brusilow, S.W. Phenylacetylglutamine may replace urea as a vehicle for waste nitrogen excretion. Pediatr. Res. 29, 147–150 (1991).
5. Nagasaka, H., Yorifuji, T., Murayama, K., Kubota, M., Kurokawa, K., Murakami, T. et al. Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency. Eur. J. Pediatr. 165, 618–624 (2006).
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献