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), 353-359
- https://doi.org/10.1111/j.1399-0004.1973.tb01931.x
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair FolliclesScience, 1971
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- 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 functionAmerican Journal Of Medicine, 1964