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Gene|March 31, 1988
Genetic basis of hypoxanthine guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome (HPRTFlint)B L Davidson, M Pashmforoush, W N Kelley, et al.The Journal of Biological Chemistry|January 5, 1989
Human hypoxanthine-guanine phosphoribosyltransferase deficiency. The molecular defect in a patient with gout (HPRTAshville)B L Davidson, M Pashmforoush, W N Kelley, et al.The Journal of Laboratory and Clinical Medicine|February 1, 1982
Adenine phosphoribosyltransferase in patients with disorders of purine and pyrimidine metabolismJ M Wilson, P E Daddona, T Otoadese, et al.The Journal of Biological Chemistry|December 25, 1982
Human hypoxanthine-guanine phosphoribosyltransferase. Tryptic peptides and post-translational modification of the erythrocyte enzymeJ M Wilson, L E Landa, R Kobayashi, et al.The Journal of Biological Chemistry|May 25, 1983
Human hypoxanthine-guanine phosphoribosyltransferaseJ M Wilson, R Kobayashi, I H Fox, et al.Ciba Foundation Symposium|January 1, 1977
Characterization of human adenosine deaminaseW N Kelley, P E Daddona, M B van der WeydenScience (New York, N.Y.)|December 6, 1974
Lesch-Nyhan syndrome: evidence for abnormal adrenergic functionS Rockson, R Stone, M Van der Weyden, et al.Advances in Experimental Medicine and Biology|January 1, 1989
Lesch-Nyhan syndrome due to a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale)S Fujimori, B L Davidson, W N Kelley, et al.Arthritis and Rheumatism|November 1, 1975
Current concepts on the regulation of purine biosynthesis de novo in manW N Kelley, E W Holmes, M B Van der WeydenNeuropediatrics|August 1, 1982
Decreased amino acids in various brain areas of patients with Lesch-Nyhan syndromeD K Rassin, K G Lloyd, W N Kelley, et al.Pageof 13