A model for hyperphenylalaninaemia due to tetrahydrobiopterin deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01813895
Reference26 articles.
1. Armarego, W. L. F. and Waring, P. Preparation of 6,6-dimethyl-5,6,7,8-tetrahydropterin hydrochloride.Aust. J. Chem. 34 (1981) 1921–1933
2. Bailey, S. W. and Ayling, J. E. 6,6-dimethylpterins: Stable quinoid dihydropterin substrate for dihydropteridine reductase and tetrahydropterin cofactor for phenylalanine hydroxylase.Biochemistry 22 (1984) 1790–1798
3. Brautigam, M., Dreesen, R. and Herken, H. Tetrahydrobiopterin and total biopterin content of neuroblastoma (NIE-115, N2A) and pheochromocytoma (PC-12) clones and the dependence of catecholamine synthesis on tetrahydrobiopterin concentration in PC-12 cells.J. Neurochem. 42 (1984) 390–396
4. Cotton, R. G. H. Inborn errors of pterin metabolism. In Blakley, R. L. (ed.)Folates and Pterins, Vol. 3, Chapter XII. Wiley, New York, 1985. (in press)
5. Curtius, H., Muldner, H. and Niederweiser, A. Tetrahydrobiopterin: Efficacy in endogenous depression and Parkinson's disease.J. Neurol. Trans. 55 (1982) 301–308
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