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Association of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's Disease

2020-06-28 genetic and genomic medicine Title + abstract only
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Rare mutations in genes originally discovered in multi-generational families have been associated with increased risk of Parkinsons Disease (PD). The involvement of rare variants in DNAJC13, UCHL1, HTRA2, GIGYF2 and EIF4G1 loci have been poorly studied or produced conflicting results across cohorts. However, they are still being often referred to as "PD-genes" and used in different models. To further elucidate the role of these five genes in PD, we fully sequenced them using molecular inversion ...

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