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]
Producer: 20200319Description: 568-580 p. digitalISSN:- 2352-3964
- 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
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Publication Type: Journal Article
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