Article ID Journal Published Year Pages File Type
8285488 Parkinsonism & Related Disorders 2018 8 Pages PDF
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.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Authors
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