The impact of rare variants in FUS in essential tremor
Movement Disorders2015Vol. 30(5), pp. 721–724
Citations Over TimeTop 21% of 2015 papers
Franziska Hopfner, Giovanni Stévanin, Stefanie H. Müller, Emeline Mundwiller, May Bungeroth, Alexandra Dürr, Manuela Pendziwiat, Mathieu Anheim, Susanne A. Schneider, Lukas Tittmann, Stephan Klebe, Delia Lorenz, Günther Deuschl, Alexis Brice, Gregor Kuhlenbäumer
Abstract
Our findings provide no evidence for a role of rare genetic variants in the pathogenesis of ET, apart from the initially published FUS mutation segregating in a large ET family.
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