The <scp> <i>LRRK2</i> G2385R </scp> Exonic Variant: A Potential Genetic Disease Modifier of Multiple System Atrophy?
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Authors
- Lucía Schottlaender
- Anne Pavy‐Le Traon (ORCID: https://orcid.org/0000-0002-9375-1553)
- O. RASCOL
- Alexandra Foubert‐Samier
- Henry Houlden
- Margherita Fabbri
- Florian Chanquoy
- David Bendetowicz
- Wassilios G. Meissner
- Nesrine Kouki
Institutions
- Centre National de la Recherche Scientifique (FR)
- Université Toulouse III - Paul Sabatier (FR)
- Université de Bordeaux (FR)
- Inserm (FR)
- Université Fédérale de Toulouse Midi-Pyrénées (FR)
- Austral University (AR)
- Centre Hospitalier Universitaire de Bordeaux (FR)
- Institut des Maladies Neurodégénératives (FR)
- New Zealand Brain Research Institute (NZ)
- Hospital Universitario Austral (AR)
- Nicolae Testemițanu State University of Medicine and Pharmacy (MD)
- National Hospital for Neurology and Neurosurgery (GB)
- University College London (GB)
Publication Details
- Journal
- Movement Disorders
- Published
- 2026-02-09
- DOI
- https://doi.org/10.1002/mds.70219
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00