Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews

To date, only one genome-wide study has assessed the contribution of copy number variants (CNVs) to Parkinson's disease (PD). We conducted a genome-wide scan for CNVs in a case–control dataset of Ashkenazi Jewish (AJ) origin (268 PD cases and 178 controls). Using high-confidence CNVs, we examin...

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Detalles Bibliográficos
Autores principales: Liu, Xinmin, Cheng, Rong, Ye, Xin, Verbitsky, Miguel, Kisselev, Sergey, Mejia-Santana, Helen, Louis, Elan D, Cote, Lucien J, Andrews, Howard F, Waters, Cheryl H, Ford, Blair, Fahn, Stanley, Marder, Karen, Lee, Joseph H, Clark, Lorraine N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782064/
https://www.ncbi.nlm.nih.gov/pubmed/24073418
http://dx.doi.org/10.1002/mgg3.18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782064/
https://www.ncbi.nlm.nih.gov/pubmed/24073418
http://dx.doi.org/10.1002/mgg3.18

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