Pentanucleotide Repeat-Related Disorders: Genetics and Bioinformatic Discovery and Detection
- Author(s)
- Silveira, I; Bennett, MF;
- Journal Title
- Epilepsia
- Abstract
- In recent years a large group of familial epilepsies and hereditary ataxias is emerging, caused by an extraordinary type of a novel pentanucleotide repeat expansion that has arisen in a preexisting non-pathogenic repeat tract. Remarkably, these insertions have occurred in non-coding regions of genes expressed in the cerebellum, but with highly diverse functions. These conditions, clinically very heterogeneous, may remain underdiagnosed in patients with atypical phenotypes and age of onset. They share, however, many genetic and phenotypic features and discovery or detection of their pathogenic pentanucleotide repeats for diagnostic purposes can be achieved using recent bioinformatic methods. Here, we focus on the latest advances regarding the peculiar group of pentanucleotide repeat-related disorders beyond epilepsies.
- Publisher
- Wiley
- Keywords
- Humans; Spinocerebellar Ataxias/genetics/pathology; Nerve Tissue Proteins/genetics; Cerebellum/pathology; Microsatellite Repeats; ATTTC insertion; Canvas; Fame; pentanucleotide repeat expansion; spinocerebellar ataxia
- Research Division(s)
- Population Health And Immunity
- PubMed ID
- 36960686
- Publisher's Version
- https://doi.org/10.1111/epi.17593
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2023-04-13 11:09:55
Last Modified: 2023-06-30 02:19:25