 | Up a level |
Krueger, Clara and Lim, Shen-Yang and Buhrmann, Alissa and Fahrig, Fenja L. and Gabbert, Carolin and Bahr, Natascha and Madoev, Harutyun and Marras, Connie and Klein, Christine and Lohmann, Katja (2025) Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson<acute accent>s disease. NPJ Parkinson's Disease, 11 (1). p. 30. ISSN 2373-8057, DOI https://doi.org/10.1038/s41531-025-00881-9.
Junker, Johanna and Lange, Lara M. and Vollstedt, Eva-Juliane and Roopnarain, Karisha and Doquenia, Maria Leila M. and Annuar, Azlina Ahmad and Avenali, Micol and Bardien, Soraya and Bahr, Natascha and Ellis, Melina and Galandra, Caterina and Gasser, Thomas and Heutink, Peter and Illarionova, Anastasia and Kanana, Yuliia and Sarmiento, Ignacio J. Keller and Kumar, Kishore R. and Lim, Shen-Yang and Madoev, Harutyun and Mata, Ignacio F. and Mencacci, Niccolo E. and Nalls, Mike A. and Padmanabhan, Shalini and Shambetova, Cholpon and Solle, J. C. and Tan, Ai-Huey and Trinh, Joanne and Valente, Enza Maria and Singleton, Andrew and Blauwendraat, Cornelis and Lohmann, Katja and Fang, Zih-Hua and Klein, Christine (2024) Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale. Movement Disorders, 39 (10). pp. 1868-1873. ISSN 0885-3185, DOI https://doi.org/10.1002/mds.29925.
