Bone Marrow Transplantation in Lesch-Nyhan Disease
- 1 January 1986
- book chapter
- Published by Springer Nature in Advances in experimental medicine and biology
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Isolation of a genomic clone partially encoding human hypoxanthine phosphoribosyltransferase.Proceedings of the National Academy of Sciences, 1982
- Hypoxanthine‐guanine phosphoribosyltransferase variants: Correlation of clinical phenotype with enzyme activityJournal of Inherited Metabolic Disease, 1981
- Disorder of purine metabolism due to partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: A study of a familyThe American Journal of Medicine, 1970
- Hemizygous Expression of Glucose-6-Phosphate Dehydrogenase in Erythrocytes of Heterozygotes for the Lesch-Nyhan SyndromeProceedings of the National Academy of Sciences, 1970
- Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in GoutAnnals of Internal Medicine, 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