The <scp> <i>LRRK2</i> G2385R </scp> Exonic Variant: A Potential Genetic Disease Modifier of Multiple System Atrophy?
- DOI
- 10.1002/mds.70219
- Published
- 2026-02-09
- Container
- Movement Disorders
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/mds.70219,
title = {The
<scp>
<i>LRRK2</i>
G2385R
</scp>
Exonic Variant: A Potential Genetic Disease Modifier of Multiple System Atrophy?},
author = {Nesrine Kouki and Anne Pavy‐Le Traon and Viorica Chelban and Florian Chanquoy and Margherita Fabbri and David Bendetowicz and Henry Houlden and Lucia V. Schottlaender and Olivier Rascol and Alexandra Foubert‐Samier and Wassilios G. Meissner},
year = {2026},
journal = {Movement Disorders},
doi = {10.1002/mds.70219},
url = {https://doi.org/10.1002/mds.70219}
}RIS
TY - JOUR
TI - The
<scp>
<i>LRRK2</i>
G2385R
</scp>
Exonic Variant: A Potential Genetic Disease Modifier of Multiple System Atrophy?
AU - Nesrine Kouki
AU - Anne Pavy‐Le Traon
AU - Viorica Chelban
AU - Florian Chanquoy
AU - Margherita Fabbri
AU - David Bendetowicz
AU - Henry Houlden
AU - Lucia V. Schottlaender
AU - Olivier Rascol
AU - Alexandra Foubert‐Samier
AU - Wassilios G. Meissner
PY - 2026
JO - Movement Disorders
DO - 10.1002/mds.70219
UR - https://doi.org/10.1002/mds.70219
ER - APA
Kouki, N., Traon, A. P., Chelban, V., Chanquoy, F., Fabbri, M., Bendetowicz, D., Houlden, H., Schottlaender, L. V., Rascol, O., Foubert‐Samier, A., & Meissner, W. G. (2026). The <scp> <i>LRRK2</i> G2385R </scp> Exonic Variant: A Potential Genetic Disease Modifier of Multiple System Atrophy?. Movement Disorders. https://doi.org/10.1002/mds.70219
Source records
- crossref · retrieved 2026-09-25T19:17:58.139Z