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...
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Glavni autori: | William J. Arnold, Jean C. Meade, William N. Kelley |
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Format: | Artigo |
Jezik: | engleski |
Izdano: |
1972
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Online pristup: | https://doi.org/10.1172/jci106982 http://www.jci.org/articles/view/106982/files/pdf |
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Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome
od: Arnold, William J., i dr.
Izdano: (1972) -
Studies on Hypoxanthine-Guanine Phosphoribosyltransferase in Fibroblasts from Patients with the Lesch-Nyhan Syndrome
od: William N. Kelley, i dr.
Izdano: (1971) -
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome.
od: Wilson, J M, i dr.
Izdano: (1983) -
Radioimmune determination of hypoxanthine phosphoribosyltransferase crossreacting material in erythrocytes of Lesch-Nyhan patients.
od: Ghangas, G S, i dr.
Izdano: (1975) -
Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome.
od: Fujimori, S, i dr.
Izdano: (1989)