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Molecular Phenotypes of Mitochondrial Dysfunction in Clinically Non-Manifesting Heterozygous PRKN Variant Carriers

Maria Paulina Castelo Rueda,Alessandra Zanon,Valentina Gilmozzi,Alexandros A. Lavdas,Athina Raftopoulou,Sylvie Delcambre,Fabiola Del Greco M,Christine Klein,Anne Grünewald,Peter P. Pramstaller,Andrew A. Hicks,Irene Pichler

npj Parkinson s Disease（2023）

Cited 8|Views40
Key words
Mutation,Parkinson's disease,Biomedicine,general,Neurosciences,Neurology
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