Article
FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees.
Neurogenetics - 1 Jan 2022
Brenner David, Müller Kathrin, Lattante Serena, Yilmaz Rüstem, Knehr Antje, Freischmidt Axel, Ludolph Albert C, Andersen Peter M, Weishaupt Jochen H
Abstract excerpt
Mutations in FUS and TBK1 often cause aggressive early-onset amyotrophic lateral sclerosis (ALS) or a late-onset ALS and/or frontotemporal dementia (FTD) phenotype, respectively. Co-occurrence of mutations in two or more Mendelian ALS/FTD genes has been repeatedly reported. However, little is known how two pathogenic ALS/FTD mutations in the same patient interact to shape the final phenotype. We screened 28 ALS...
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