FUS in familial essential tremor - The search for common causes is still on
Abstract
The genetic etiology of essential tremor remains unknown despite the significant proportion of familial cases. The search for monogenic causes has repeatedly failed until recent identification of three disease-causing mutations in FUS (fused in sarcoma), a gene previously linked to a rare forms of familial amyotrophic lateral sclerosis with frontotemporal dementia. The genetic epidemiology of FUS in ET is unknown. Herein, we screened 104 patients from 52 pedigrees for mutations in the coding sequence of FUS. Two of the most genetically distant affected individuals from each pedigree were selected for Sanger sequencing to potentially increase the success of genetic analysis. We did not identify a single pathogenic mutation. Our data suggest that FUS mutations are a rare cause of familial ET. © 2013 Elsevier Ltd.
Publication Title
Parkinsonism and Related Disorders
Recommended Citation
Hedera, P., Davis, T., Phibbs, F., Charles, P., & LeDoux, M. (2013). FUS in familial essential tremor - The search for common causes is still on. Parkinsonism and Related Disorders, 19 (9), 818-820. https://doi.org/10.1016/j.parkreldis.2013.04.009
