Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 families*
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1977.tb01299.x/fullpdf
Reference18 articles.
1. Activation of variants of hypoxanthine-guanine phosphoribosyl transferase by normal enzyme;Bakay;Proc. nat. Acad. Sci. (Wash.),1972
2. Heterogeneity of hypoxanthine-guanine phosphoribosyl transferase from human erythrocytes;Bakay;Arch. Biochem. Biophys.,1975
3. Hypoxanthine-guanine phosphoribosyl transferase variant associated with accelerated purine synthesis;Benke;J. clin. Invest.,1973a
4. Transport of hypoxanthine in fibroblasts with normal and mutant hypoxanthine-guanine phosphoribosyl transferase;Benke;Biochem. Med.,1973b
5. Hypoxanthineguanine phosphoribosyl transferase deficiency;Bruyn;Hum. Genet.,1976
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1. Monoamine oxidase and catechol-o-m ethyl transferase activity in cultured fibroblasts from patients with maple syrup urine disease, Lesch-Nyhan syndrome and healthy controls;Clinical Genetics;2008-04-23
2. Experimental models;Arthritis & Rheumatism;1981-02
3. Disorders of Purine and Pyrimidine Metabolism;Contemporary Metabolism;1979
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