Hypoxanthine guanine phosphoribosyl transferase deficiency presenting with gout and renal failure in infancy.

Author:

Holland P C,Dillon M J,Pincott J,Simmonds H A,Barratt T M

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference6 articles.

1. A familial disorder of uric acid metabolism and central nervous system function;Lesch, M.; Nyhan, W.L.;Amer J Med,1964

2. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis;Seegmiller, J.E.; Rosenbloom, F.M.; Kelley, W.N.;Science,1967

3. Clinical syndromes associated with hypoxanthine guanine phosphoribosyl transferase deficiency;Kelley, W.N.; Wyngarden, J.D.

4. Disparate enzyme activity in erythrocytes and leukocytes;Dancis, J.; Yip, L.C.; Cox, R.P.; Piomelli, S.; Balis, M.E.;J Clin Invest,1973

5. The spectrum of hypoxanthine-guanine phosphoribosyl transferase deficiency;Emmerson, B.T.; Thompson, L.;QJ Med,1973

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