Study of Korean Parkinson's disease
Single nucleotide variants (SNVs) associated with Parkinson’s disease (PD) have been investigated mainly through genome-wide association studies. Here, we conducted whole genome sequencing of 410 PD patients and 200 healthy individuals of the Korean population and identified disease-related SNVs.
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00001009775 | 1 |
| Publications | Citations |
|---|---|
|
Whole-genome sequencing reveals an association between small genomic deletions and an increased risk of developing Parkinson's disease.
Exp Mol Med 55: 2023 555-564 |
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