| 1 |
33098802 | Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies. | 2020 Nov |
1 |
| 2 |
31607598 | A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. | 2019 Oct |
1 |
| 3 |
24751306 | Association of premenstrual/menstrual symptoms with perinatal depression and a polymorphic repeat in the polyglutamine tract of the retinoic acid induced 1 gene. | 2014 Jun |
1 |
| 4 |
22868089 | ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia. | 2012 Oct 15 |
1 |