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Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

4 Mar 2019

Abstract excerpt

Genetic studies of the familial forms of Parkinson's disease (PD) have identified a number of causative genes with an established role in its pathogenesis. These genes only explain a fraction of the diagnosed cases. The emergence of Next Generation Sequencing (NGS) expanded the scope of rare variants identification in novel PD related genes. In this study we describe whole exome sequencing (WES) genetic findings...

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PMID: 30833663
DOI: 10.1038/s41598-019-40102-x

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