Genetic risk factor clustering within and across neurodegenerative diseases

Overlapping symptoms and co-pathologies are common in closely related neurodegenerative diseases (NDDs). Investigating genetic risk variants across these NDDs can give further insight into disease manifestations. In this study we have leveraged genome-wide single nucleotide polymorphisms and genome-...

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Detalles Bibliográficos
Autores principales: Koretsky, Mathew J, Alvarado, Chelsea, Makarious, Mary B, Vitale, Dan, Levine, Kristin, Bandres-Ciga, Sara, Dadu, Anant, Scholz, Sonja W, Sargent, Lana, Faghri, Faraz, Iwaki, Hirotaka, Blauwendraat, Cornelis, Singleton, Andrew, Nalls, Mike, Leonard, Hampton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629980/
https://www.ncbi.nlm.nih.gov/pubmed/37192343
http://dx.doi.org/10.1093/brain/awad161

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629980/
https://www.ncbi.nlm.nih.gov/pubmed/37192343
http://dx.doi.org/10.1093/brain/awad161

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