Erythrocyte Adenine PRPP Availability in Two Types of APRT Deficiency Using Silicon Oil Method

Author:

Takeuchi Fujio,Kamatani Naoyuki,Nishida Yutaro,Miyamoto Terumasa

Publisher

Springer US

Reference18 articles.

1. Cartier, P., and Hamet, M., 1974, Une nouvelle maladie metabolique: le deficit complete en adeninephosphoribosyltransferase avec lithiase de 2, 8-dihydroxyadenine, C. R. Acad. Sci. [D] (Paris), 279: 883.

2. Dean, B. M., Perret, D., Simmonds, H. A., Sahota, A., and Van Acker, K. J., 1978, Adenine and adenosine metabolism in intact erythrocytes deficient in adenine monophosphate-pyrophosphate phosphoribosyl-transferase: A study of two families, Clin. Sci. Mol. Med., 55: 407.

3. Emmerson, B. T., Gordon, R. B., and Thompson, L., 1975, Adenine phosphori-bosyltransferase deficiency in man: Its inheritance and occurrence in a female with gout and renal disease, Aust. N. Z. J. Med., 5: 440.

4. Fox, I. H., Meade, J. C., and Kelly, W. N., 1973, Adenine phosphoribosyl-transferase deficiency in man. Report of a second family, Am. J. Med., 55: 614.

5. Fox, I. H., La Croix, S., Planet, G., and Moore, M., 1977, Partial deficiency of adenine phosphoribosyltransferase in man, Medicine, 56: 515.

Cited by 1 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

1. The Clinical Aspects of APRT Deficiency;Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism;1993

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