Whole-genome sequencing reveals an association between small genomic deletions and an increased risk of developing Parkinson’s disease

Single-nucleotide variants (SNVs) associated with Parkinson’s disease (PD) have been investigated mainly through genome-wide association studies. However, other genomic alterations, including copy number variations, remain less explored. In this study, we conducted whole-genome sequencing of primary...

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Detalles Bibliográficos
Autores principales: Oh, Ji-Hye, Jo, Sungyang, Park, Kye Won, Lee, Eun-Jae, Lee, Seung Hyun, Hwang, Yun Su, Jeon, Ha Ra, Ryu, Yeonjin, Yoon, Hee Jeong, Chun, Sung-Min, Kim, Chong Jai, Kim, Tae Won, Sung, Chang Ohk, Chae, Sehyun, Chung, Sun Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073127/
https://www.ncbi.nlm.nih.gov/pubmed/36869069
http://dx.doi.org/10.1038/s12276-023-00952-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073127/
https://www.ncbi.nlm.nih.gov/pubmed/36869069
http://dx.doi.org/10.1038/s12276-023-00952-y

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