An atypical case of hypoxanthine‐guanine phosphoribosyltransferase deficiency (Lesch‐Nyhan syndrome)
- 1 July 1973
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 4 (4) , 348-352
- https://doi.org/10.1111/j.1399-0004.1973.tb01930.x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- An atypical case of hypoxanthine‐guanine phosphoribosyltransferase deficiency (Lesch‐Nyhan syndrome)Clinical Genetics, 1973
- Clinical Features of the Lesch-Nyhan SyndromeArchives of internal medicine (1960), 1972
- CONCENTRATION OF PURINE NUCLEOTIDES IN ERYTHROCYTES OF PATIENTS WITH THE LESCH‐NYHAN SYNDROME BEFORE AND DURING ORAL ADMINISTRATION OF ADENINEActa Paediatrica, 1971
- Purine Metabolism in Heterozygous Carriers of Hypoxanthine-Guanine Phosphoribosyltransferase DeficiencyScience, 1969
- Synthesis of an enzyme determined by an erythrocyte nucleus in a hybrid cellJournal of Cell Science, 1969
- Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine SynthesisScience, 1967
- A familial disorder of uric acid metabolism and central nervous system functionThe American Journal of Medicine, 1964
- The Measurement and Appraisal of Adult Intelligence (4th ed.).Published by American Psychological Association (APA) ,1958