RIC3 variants are not associated with Parkinson’s disease in large European, Latin American, or East Asian cohorts

Parkinson’s disease (PD) is a complex neurodegenerative disorder in which both rare and common genetic variants contribute to disease risk. Multiple genes have been reported to be linked to monogenic PD but these only explain a fraction of the observed familial aggregation. Rare variants in RIC3 hav...

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Detalles Bibliográficos
Autores principales: Brolin, Kajsa, Bandres-Ciga, Sara, Leonard, Hampton, Makarious, Mary B., Blauwendraat, Cornelis, Mata, Ignacio F, Foo, Jia Nee, Pihlstrøm, Lasse, Swanberg, Maria, Gan-Or, Ziv, Tan, Manuela MX
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011339/
https://www.ncbi.nlm.nih.gov/pubmed/34538707
http://dx.doi.org/10.1016/j.neurobiolaging.2021.08.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011339/
https://www.ncbi.nlm.nih.gov/pubmed/34538707
http://dx.doi.org/10.1016/j.neurobiolaging.2021.08.009

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