| Literature DB >> 34537679 |
Yevgenya Abramzon1, Ramita Dewan2, Andrea Cortese3, Susan Resnick4, Luigi Ferrucci5, Henry Houlden6, Bryan J Traynor7.
Abstract
A homozygous AAGGG repeat expansion within the RFC1 gene was recently described as a common cause of CANVAS syndrome. We examined 1069 sporadic ALS patients for the presence of this repeat expansion. We did not discover any carriers of the homozygous AAGGG expansion in our ALS cohort, indicating that this form of RFC1 repeat expansions is not a common cause of sporadic ALS. However, our study did identify a novel repeat conformation and further expanded on the highly polymorphic nature of the RFC1 locus.Entities:
Keywords: ALS; Motor neuron disorders; RFC1
Mesh:
Substances:
Year: 2021 PMID: 34537679 PMCID: PMC9014296 DOI: 10.1016/j.jns.2021.118061
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 4.553