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...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | inglés |
| Publicado: |
1971
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| Acceso en línea: | https://doi.org/10.1016/s0021-9258(18)62275-6 |
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