Back to Search
Start Over
No biallelic intronic AAGGG repeat expansion in RFC1 was found in patients with late-onset ataxia and MSA.
- Source :
-
Parkinsonism & related disorders [Parkinsonism Relat Disord] 2020 Apr; Vol. 73, pp. 1-2. Date of Electronic Publication: 2020 Feb 26. - Publication Year :
- 2020
-
Abstract
- We screened the RFC1 intronic AAGGG repeat expansions in late-onset ataxia cases, MSA patients and controls. The data suggested that no biallelic repeat expansion carrier was found in our cohort and the heterozygous intronic AAGGG repeat expansions may not lead to an increased risk of late-onset ataxia or MSA.<br />Competing Interests: Declaration of competing interest None.<br /> (Copyright © 2020. Published by Elsevier Ltd.)
Details
- Language :
- English
- ISSN :
- 1873-5126
- Volume :
- 73
- Database :
- MEDLINE
- Journal :
- Parkinsonism & related disorders
- Publication Type :
- Report
- Accession number :
- 32151945
- Full Text :
- https://doi.org/10.1016/j.parkreldis.2020.02.017