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...
保存先:
主要な著者: | William J. Arnold, Jean C. Meade, William N. Kelley |
---|---|
フォーマット: | Artigo |
言語: | 英語 |
出版事項: |
1972
|
オンライン・アクセス: | https://doi.org/10.1172/jci106982 http://www.jci.org/articles/view/106982/files/pdf |
タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|
類似資料
-
Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome
著者:: Arnold, William J., 等
出版事項: (1972) -
Studies on Hypoxanthine-Guanine Phosphoribosyltransferase in Fibroblasts from Patients with the Lesch-Nyhan Syndrome
著者:: William N. Kelley, 等
出版事項: (1971) -
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome.
著者:: Wilson, J M, 等
出版事項: (1983) -
Radioimmune determination of hypoxanthine phosphoribosyltransferase crossreacting material in erythrocytes of Lesch-Nyhan patients.
著者:: Ghangas, G S, 等
出版事項: (1975) -
Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome.
著者:: Fujimori, S, 等
出版事項: (1989)