Page last updated: 2024-08-24

5-methylcytosine and Lesch-Nyhan Syndrome

5-methylcytosine has been researched along with Lesch-Nyhan Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Finette, BA; O'Neill, JP	1

Reviews

1 review(s) available for 5-methylcytosine and Lesch-Nyhan Syndrome

Article	Year
Transition mutations at CpG dinucleotides are the most frequent in vivo spontaneous single-based substitution mutation in the human HPRT gene. Environmental and molecular mutagenesis, 1998, Volume: 32, Issue:2 Topics: 5-Methylcytosine; Adult; Child; CpG Islands; Cytosine; DNA Mutational Analysis; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Infant, Newborn; Lesch-Nyhan Syndrome; Male; Point Mutation	1998

Article

Year

Transition mutations at CpG dinucleotides are the most frequent in vivo spontaneous single-based substitution mutation in the human HPRT gene.

Environmental and molecular mutagenesis, 1998, Volume: 32, Issue:2

Topics: 5-Methylcytosine; Adult; Child; CpG Islands; Cytosine; DNA Mutational Analysis; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Infant, Newborn; Lesch-Nyhan Syndrome; Male; Point Mutation

1998