Cargando…
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
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: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499986/ https://www.ncbi.nlm.nih.gov/pubmed/37704671 http://dx.doi.org/10.1038/s41531-023-00560-7 |
Ejemplares similares
-
Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
por: Lange, Lara M., et al.
Publicado: (2023) -
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
por: Towns, Clodagh, et al.
Publicado: (2023) -
Mendelian Randomization — the Key to Understanding Aspects of Parkinson's Disease Causation?
por: Noyce, Alastair J., et al.
Publicado: (2015) -
Glucocerebrosidase Defects as a Major Risk Factor for Parkinson’s Disease
por: Avenali, Micol, et al.
Publicado: (2020) -
Genetic Testing for
GBA
and
LRRK2
Mutations: Is it Time for Routine Use?
por: Roopnarain, Karisha, et al.
Publicado: (2023)