| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8285425 | Parkinsonism & Related Disorders | 2018 | 17 Pages |
Abstract
Carriers of the LRRK2 p.N551K-p.R1398H-p.K1423K haplotype have a reduced risk for developing RBD, yet PD-causing mutations probably have minor or no role in RBD. Additional work is needed to confirm these results and to identify the mechanism associated with reduced risk for RBD.
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Authors
Bouchra Ouled Amar Bencheikh, Jennifer A. Ruskey, Isabelle Arnulf, Yves Dauvilliers, Christelle Charley Monaca, Valérie Cochen De Cock, Jean-François Gagnon, Dan Spiegelman, Michele T.M. Hu, Birgit Högl, Ambra Stefani, Luigi Ferini-Strambi,