Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

The Monogenic Network of the Global Parkinson’s Genetics Program (GP2) aims to create an efficient infrastructure to accelerate the identification of novel genetic causes of Parkinson’s disease (PD) and to improve our understanding of already identified genetic causes, such as reduced penetrance and...

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Detalles Bibliográficos
Autores principales: Lange, Lara M., Avenali, Micol, Ellis, Melina, Illarionova, Anastasia, Keller Sarmiento, Ignacio J., Tan, Ai-Huey, Madoev, Harutyun, Galandra, Caterina, Junker, Johanna, Roopnarain, Karisha, Solle, Justin, Wegel, Claire, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore R., Lim, Shen-Yang, Valente, Enza Maria, Nalls, Mike, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, Niccolo, Lohmann, Katja, Klein, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300084/
https://www.ncbi.nlm.nih.gov/pubmed/37369645
http://dx.doi.org/10.1038/s41531-023-00526-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300084/
https://www.ncbi.nlm.nih.gov/pubmed/37369645
http://dx.doi.org/10.1038/s41531-023-00526-9

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