Author:
Shi Zheng-Zheng,Habib Geetha M.,Rhead William J.,Gahl William A.,He Xiangwei,Sazer Shelley,Lieberman Michael W.
Publisher
Springer Science and Business Media LLC
Reference22 articles.
1. Jellum, E., Kluge, T., Börresen, H.C., Stokke, O. & Eldjarn, L. Pyroglutamic aciduria — A new inborn error of metabolism. Scand. J. Clin. Lab. Invest. 26, 327–335 (1970).
2. Larsson, A. et al. 5-Oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers — A new inborn error of the γ-glutamyl cycle. Acta Pediat. Scand. 70, 301–308 (1981).
3. Larsson, A. Hereditary disorders in glutathione metabolism. in Glutathione: Metabolism and physiological functions (ed. Viña, J.) 359–366 (CRC Press, Boston, 1990).
4. Meister, A. & Larsson, A. Glutathione synthetase deficiency and other disorders of the γ-glutamyl cycle. in The Metabolic basis of inherited disease, 7th edn. (eds Beaudet, A.L., Scriver, C.R., Sly, W. S. & Valle, D.) 1461–1477 (McGraw-Hill, New York, 1995).
5. Spielberg, S.P. et al. 5-Oxoprolinuria: biochemical observations and case report. J. Pediat. 91, 237–241 (1977).
Cited by
83 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