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...
Shranjeno v:
Main Authors: | , |
---|---|
Format: | Artigo |
Jezik: | angleščina |
Izdano: |
1971
|
Online dostop: | https://doi.org/10.1016/s0021-9258(18)62275-6 |
Oznake: |
Označite
Brez oznak, prvi označite!
|