Hypoxanthine-guanine phosphoribosyl transferase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00296142.pdf
Reference130 articles.
1. Adams, A., Anderson, J. M., Nicol, A. D., Harkness, A.: The development of hypoxanthine-guanine phosphoribosyl transferase in man. Biochem. J. 125, 36 (1971)
2. Albertini, R. J., De Mars, R.: Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation. Biochem. Genet. 11, 397?411 (1974)
3. Andrews, T. M., Tata, J. R.: Protein synthesis by membrane bound and free ribosomes of the developing rat cerebral cortex. Biochem. J. 124, 883?889 (1971)
4. Arnold, W. J., Kelley, W. N.: Human hypoxanthine-guanine phosphoribosyl transferase: purification and subunit structure. J. biol. Chem. 246, 7398?7404 (1971)
5. Arnold, W. J., Mead, J. C., Kelley, W. N.: Hypoxanthine-guanine phosphoribosyl transferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome. J. clin. Invest. 51, 1805?1812 (1972)
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