Studies on Hypoxanthine-Guanine Phosphoribosyltransferase in Fibroblasts from Patients with the Lesch-Nyhan Syndrome
Abstract The Lesch-Nyhan syndrome has been characterized by an apparently complete deficiency in erythrocytes of an enzyme of purine metabolism, hypoxanthine-guanine phosphoribosyl-transferase. Recent studies have suggested that low levels of this enzyme may be present in skin fibroblasts cultured f...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | englanti |
| Julkaistu: |
1971
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| Linkit: | https://doi.org/10.1016/s0021-9258(18)62275-6 |
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