Article

Integrated Sequencing & Array Comparative Genomic Hybridization in Familial Parkinson’s Disease

2019-11-11

Abstract excerpt

<h4>Background</h4> Parkinson’s disease (PD) is a genetically heterogeneous condition; both single nucleotide variants (SNVs) and copy number variants (CNVs) are important genetic risk factors. We examined the utility of combining exome sequencing and genome-wide array-based comparative genomic hybridization (aCGH) for identification of PD genetic risk factors. <h4>Methods</h4> We performed exome sequencing on 1...

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Literature Corpus work: 770bd238-1797-515a-b357-dbba1d539668
DOI: 10.1101/828566

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