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Genome-wide association study of copy number variations in Parkinson’s disease

Landoulsi Z, Ashok Kumar Sreelatha A, Kuznetsov N, Schulte C, Bobbili DR, Montanucci L, Leu C, Niestroj L, Hassanin E, Domenighetti C, Sugier P, Radivojkov-Blagojevic M, Lichtner P, Portugal B, Edsall C, Kru□ger J, Hernandez DG, Blauwendraat C, Mellick GD, Zimprich A, Pirker W, Tan M, Rogaeva E, Lang A, Koks S, Taba P, Lesage S, Brice A, Corvol J, Chartier-Harlin M, Mutez E, Brockmann K, Deutschländer AB, Hadjigeorgiou GM, Dardiotis E, Stefanis L, Simitsi AM, Valente EM, Petrucci S, Straniero L, Zecchinelli A, Pezzoli G, Brighina L, Ferrarese C, Annesi G, Quattrone A, Gagliardi M, Burbulla LF, Matsuo H, Nakayama A, Hattori N, Nishioka K, Chung SJ, Kim YJ, Pavelka L, Kolber P, van de Warrenburg BP, Bloem BR, Singleton AB, Vitale D, Toft M, Pihlstrom L, Guedes LC, Ferreira JJ, Bardien S, Carr J, Tolosa E, Ezquerra M, Pastor P, Wirdefeldt K, Pedersen NL, Ran C, Belin AC, Puschmann A, Clarke CE, Morrison KE, Krainc D, Farrer MJ, Lal D, the Global Parkinson Genetics Program (GP2), Elbaz A, Gasser T, Krüger R, Sharma M, May P.

· 2024-08-22

DOI: 10.1101/2024.08.21.24311915

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

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