Whole Exome Sequencing in Familial Parkinson Disease

Study ID Alternative Stable ID Type
phs000376 Family

Study Description

We have an ongoing study that has recruited families having at least a sibling pair with Parkinson disease (PD). Families have been screened for mutations in known PD causative genes (LRRK2, parkin, etc). Following review of families without a causative mutation, we selected families for whole exome sequencing that had the strongest history of PD and with the most definitive diagnosis. All families have at least 3 affected family members who were evaluated as part of this study. Only affected family members were included for whole exome sequencing.

Archive Link Archive Accession
dbGaP phs000376

Who archives the data?

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