Genome-wide association study of copy number variations in Parkinson's disease
Z. Landoulsi, A. A.K. Sreelatha, Kuznetsov N., C. Schulte et autres
We investigated the role of copy number variations (CNVs) in Parkinson’s disease (PD) using genotyping data from 10,815 patients (2731 early-onset PD, EOPD) and 8901 controls from the COURAGE-PD consortium. CNVs were analyzed using a sliding window genome-wide association and burden approach. …