A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. [electronic resource]
- EBioMedicine Oct 2019
- 568-580 p. digital
Publication Type: Journal Article
2352-3964
10.1016/j.ebiom.2019.09.020 doi
Adolescent Adult Aged Aged, 80 and over Alleles Child DNA Repair Exons Female Genetic Predisposition to Disease Genotype Humans Huntingtin Protein--genetics Huntington Disease--diagnosis Male Middle Aged Polymorphism, Single Nucleotide Quantitative Trait Loci Trinucleotide Repeat Expansion Young Adult