The LRRK2 G2385R Exonic Variant: A Potential Genetic Disease Modifier of Multiple System Atrophy?

Movement Disorders 2026

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Authors: Nesrine Kouki, Anne Pavy‐Le Traon, Viorica Chelban, Florian Chanquoy, Margherita Fabbri, David Bendetowicz, Henry Houlden, Lucía Schottlaender, O. RASCOL, Alexandra Foubert‐Samier, Wassilios G. Meissner
DOI: 10.1002/mds.70219
Cited by: 2
References: 6

Abstract

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions. Data S1. Supporting Information. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Fields of Study & Subjects

Genetic Neurodegenerative Diseases Parkinson's Disease Mechanisms and Treatments Neurological diseases and metabolism

Publication details

Journal / source
Movement Disorders
Publisher
Wiley
Volume
41
Issue
3
Pages
792–794
Publication date
9 February 2026
Language
EN