Mutational analysis of COQ2 in patients with MSA in Italy
- PMID: 27394078
- DOI: 10.1016/j.neurobiolaging.2016.05.022
Mutational analysis of COQ2 in patients with MSA in Italy
Abstract
COQ2 mutations have been implicated in the etiology of multiple system atrophy (MSA) in Japan. However, several genetic screenings have not confirmed the role of its variants in the disease. We performed COQ2 sequence analysis in 87 probable MSA. A homozygous change p.A43G was found in an MSA-C patient. Cosegregation analysis and the evaluation of CoQ10 content in muscle and fibroblasts did not support the pathogenic role of this variant.
Keywords: COQ2; CoQ10; MSA.
Copyright © 2016 Elsevier Inc. All rights reserved.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources