Human Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency
Open Access
- 1 January 1989
- journal article
- Published by Elsevier
- Vol. 264 (1) , 520-525
- https://doi.org/10.1016/s0021-9258(17)31289-9
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Human hypoxanthine-guanine phosphoribosyltransferase: a single nucleotide substitution in cDNA clones isolated from a patient with Lesch-Nyhan syndrome (HPRTMidland)Gene, 1988
- Structural studies of mutants of the lysozyme of bacteriophage T4Journal of Molecular Biology, 1987
- Expression of the mouse HPRT gene: Deletional analysis of the promoter region of an X-Chromosome linked housekeeping geneCell, 1985
- Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.Journal of Clinical Investigation, 1985
- Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patientsNature, 1984
- Hypoxanthine-Guanine Phosphoribosyltransferase DeficiencyNew England Journal of Medicine, 1983
- Prediction of protein antigenic determinants from amino acid sequences.Proceedings of the National Academy of Sciences, 1981
- Molecular basis of thermostability in the lysozyme from bacteriophage T4Nature, 1979
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine SynthesisScience, 1967