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Deep mitochondrial sequencing in Parkinson's disease reveals possible genetic modifiers of reduced penetrance in Parkin/PINK1 mutation carriers

J. Trinh,A. Hicks,K. Wasner,M. Farrer,F. Hentati,P. Bauer, S. Imhoff,K. Kandaswamy, N. Ouzren,M. Werber,A. Rolfs,V. Kostic, A. Lang,P. Pramstaller,P. Seibler,K. Lohmann,A. Gruenewald,C. Klein

MOVEMENT DISORDERS（2019）

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