Repeat expansion in a fragile X model is independent of double strand break repair mediated by Pol θ, RAD52, RAD54 or RAD54B
Bruce E. Hayward(National Institutes of Health), Karen Usdin(National Institute of Diabetes and Digestive and Kidney Diseases)
Cited by 2
Related Papers
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection
|Nature Genetics|2006|673
Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome
|The American Journal of Human Genetics|2007|449
The biological effects of simple tandem repeats: Lessons from the repeat expansion diseases: Table 1.
|Genome Research|2008|281
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus
|Nature Genetics|2024|34