Article ID Journal Published Year Pages File Type
8285518 Parkinsonism & Related Disorders 2018 6 Pages PDF
Abstract
Point mutations in LRRK2 and SNCA are a rare cause of autosomal dominant PD in Turkey. However, copy number variations should be considered. The unclassified variants, especially LRRK2 R1067Q, demand further investigation.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Authors
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