Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8285488 | Parkinsonism & Related Disorders | 2018 | 8 Pages |
Abstract
Eighteen probands have screened negative for known CNVs and mutations that cause clear monogenic forms of PD. Each family is a candidate for further genetic analysis to identify genetic variants segregating with disease. The families enrolled in the QPP provide a useful resource to aid in identifying novel forms of monogenic PD.
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Authors
Steven R. Bentley, Stephanie Bortnick, Ilaria Guella, Javed Y. Fowdar, Peter A. Silburn, Stephen A. Wood, Matthew J. Farrer, George D. Mellick,