Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome
The Lesch-Nyhan syndrome is characterized clinically by choreoathetosis, spasticity, selfmutilation, and mental and growth retardation. Biochemically, there is a striking reduction of hypoxanthine-guanine phosphoribosyltransferase (HGPRT) activity in affected individuals. We have examined erythrocyt...
محفوظ في:
المؤلفون الرئيسيون: | William J. Arnold, Jean C. Meade, William N. Kelley |
---|---|
التنسيق: | Artigo |
اللغة: | الإنجليزية |
منشور في: |
1972
|
الوصول للمادة أونلاين: | https://doi.org/10.1172/jci106982 http://www.jci.org/articles/view/106982/files/pdf |
الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|
مواد مشابهة
-
Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome
حسب: Arnold, William J., وآخرون
منشور في: (1972) -
Studies on Hypoxanthine-Guanine Phosphoribosyltransferase in Fibroblasts from Patients with the Lesch-Nyhan Syndrome
حسب: William N. Kelley, وآخرون
منشور في: (1971) -
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome.
حسب: Wilson, J M, وآخرون
منشور في: (1983) -
Radioimmune determination of hypoxanthine phosphoribosyltransferase crossreacting material in erythrocytes of Lesch-Nyhan patients.
حسب: Ghangas, G S, وآخرون
منشور في: (1975) -
Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome.
حسب: Fujimori, S, وآخرون
منشور في: (1989)