Work

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

Year: 2026

Type: article

Source: Movement Disorders

DOI: 10.1002/mds.70219

Authors: Nesrine Kouki, Anne Pavy‐Le Traon, Viorica Chelban, Florian Chanquoy, Margherita Fabbri, David Bendetowicz, Henry Houlden, Lucia V. Schottlaender, Olivier Rascol, Alexandra Foubert‐Samier, Wassilios G. Meissner

Institutions: Centre Hospitalier Universitaire de Bordeaux, Institut des Maladies Neurodégénératives, Inserm, Centre Hospitalier Universitaire de Toulouse, Centre d’Investigation Clinique 1436, Université de Toulouse, Nicolae Testemițanu State University of Medicine and Pharmacy, National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, University College London, Université Toulouse III - Paul Sabatier, Toulouse NeuroImaging Center, Centre National de la Recherche Scientifique, Université de Bordeaux, Consejo Nacional de Investigaciones Científicas y Técnicas, Austral University, Hospital Universitario Austral, New Zealand Brain Research Institute, University of Otago

Language: English

Topic: Parkinson's Disease Mechanisms and Treatments

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W7128490030

FWCI: 8.104

Cites: 6

Cited by: 2

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