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A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease.

Kun-Rodrigues C, Ganos C, Guerreiro R, Schneider SA, Schulte C, Lesage S, Darwent L, Holmans P, Singleton A, International Parkinson's Disease Genomics Consortium (IPDGC), Bhatia K, Bras J.

Hum Mol Genet · 2015-09-11

DOI: 10.1093/hmg/ddv376PMID: 26362251

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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